Preparation and Synthetic Applications of Five-to-Seven-Membered Cyclic α-Diazo Monocarbonyl Compounds

The reactivity of cyclic α-diazo monocarbonyl compounds differs from that of their acyclic counterparts. In this review, we summarize the current literature available on the synthesis and synthetic applications of three major classes of cyclic α-diazo monocarbonyl compounds: α-diazo ketones, α-diazo lactones and α-diazo lactams.


Introduction
α-Diazocarbonyl compounds are distinctly versatile reagents for organic synthesis, capable of a wide range of synthetic transformations [1][2][3][4]. However, in contrast to more common cyclic 2-diazo-1,3-dicarbonyl compounds, five-to-seven-membered cyclic α-diazo monocarbonyl compounds (including α-diazo ketones, α-diazo lactones and α-diazo lactams) remain noticeably underexplored, both in terms of preparative methods to access them and their utility as reagents for organic synthesis. Such compounds (as well as carbene species generated therefrom) are expected to be more reactive compared to their acyclic counterparts, due to ring strain that causes, in turn, weaker conjugation of the diazo function (or the resulting carbene center) to the carbonyl group [5]. Higher reactivity may also be the reason for the lower chemical stability of α-diazo monocarbonyl compounds, which consequently hampers their preparation and use in organic synthesis. However, the range of preparative methods and synthetic applications enabling access to and the practical use of α-diazo monocarbonyl compounds has been expanding. In this review, we aim to summarize the current developments in the field of cyclic α-diazo monocarbonyl compounds, including α-diazo-γ-butyrolactams that were recently introduced and developed as reagents for organic synthesis in our laboratories.

Methods of Synthesis of Cyclic α-Diazo Ketones
In the majority of cases, cyclic α-diazo ketones are synthesized using the general method of diazo transfer. As the acidity of the methylene group in the α-position to the carbonyl group is relatively low, the diazo transfer reaction requires fairly forceful conditions, which would lead to the other methylene group also being affected in the reaction. Therefore, to achieve a selective mono transfer of the diazo function, the ketones are preliminarily activated by formylation, and only such a monoformylated substrate is subjected to deformylative diazo transfer conditions [6][7][8][9]. This is illustrated by the preparation of mono-diazo bicyclic ketone derivative 1 (Scheme 1). Scheme 1. Example of deformylative diazo transfer in the synthesis of bicyclic α-diazo ketone 1.
In some cases, however, when the target molecule does not have a nearby methylene or methyne group with similar acidity to the target methylene group, a direct diazo transfer becomes possible, as illustrated by the synthesis of polycyclic α-diazo ketones 2 and 3 (Scheme 2) [10][11][12][13].

Scheme 2. Examples of direct diazo transfer reactions not requiring pre-formylation.
A standalone case is when a diazo transfer is employed to prepare β,γ-unsaturated α-diazo cyclic ketones, such as α-diazo cyclohex-β,γ-enones. The lowered acidity of the α-methylene group, along with the presence of the reactive double bond, mandate that the substrate is first α-trifluoroacetylated in the presence of a strong base at a low temperature. Thereupon, the de-trifluoroacetylative diazo transfer can already occur. This is illustrated by the synthesis of α-diazo δ,ε-cyclohexenone 4 (Scheme 3) [14][15][16]. The main drawback of many diazo transfer reactions is the formation of an equivalent amount of sulfonamide, which requires the target product to be chromatographically purified. This drawback can be conveniently alleviated by the recently described modification of the diazo transfer reaction termed 'sulfonyl-azide-free' (SAFE), which allows, among other things, the synthesizing of cyclic α-diazo ketones. The key to this method is the use of water-soluble 3-(chlorosulfonyl)benzoic acid as the precursor to the respective sulfonyl azide. The latter is formed in situ under the influence of sodium azide in a weakly alkaline aqueous solution. To the solution, thus formed, a formylated cyclic ketone is added and, when the reaction is over, the target α-diazo ketone is simply extracted with chloroform while the unwanted sulfonamide remains in the water. This method turns out to be applicable to the preparation of high-purity five-to-eight-membered cyclic ketones 5 in good yields, the only surprising exception being cyclohexanone (Scheme 4) [17]. The major drawback of synthesizing α-diazo ketones using the diazo transfer reaction is the need to use a strong base. If the use of such bases must be avoided for some reason, a diazo transfer could involve, not a premade enol but rather, an enamine. Such enamines are easy to synthesize using the so-called Bredereck's reagent (6) in reactions with the starting cyclic ketones. In this case, the use of a strong base is required at neither the enamine synthesis stage nor at the diazo transfer step, as illustrated, for example, by the synthesis of a rather sensitive nucleobase 7 derivative (Scheme 5) [18,19]. Scheme 5. The use of the Bredereck's reagent (6) in the activation of sensitive substrates.
In one case, one of the two carbonyl groups is turned into an oxime (such as 8) with treatment with isoamyl nitrite in a basic medium, and the resulting oxime is oxidized to a diazo group [20]. Alternatively, one of the carbonyl groups can be transformed into a tosyl hydrazone, and the resulting hydrazone (such as 9) is fragmented with a base to give the target α-diazo ketone (Scheme 6) [21][22][23]. Scheme 6. Examples of α-diazo ketone synthesis via oxime (8) and tosyl hydrazone (9) fragmentation.
A separate case is represented by the synthesis of β-hydroxy-α-diazo cyclic ketones-an important class of diazo compounds. The most common way to access such building blocks is with a base-promoted intramolecular addition of a terminal diazo ketone to another carbonyl group (as shown for the preparation of 10) [24][25][26]. More simple derivatives of this class can be accessed from the respective diazo dicarbonyl compounds (such as 11) by desymmetrizing the reduction of one of the carbonyl groups (Scheme 7) [27]. Scheme 7. Approaches to the synthesis of β-hydroxy-α-diazo cyclic ketones.

The Wolff Rearrangement of Cyclic α-Diazo Ketones
Despite the more than fifty-year history of studying the reactions of ketenes resulting from the decomposition of cyclic diazo monocarbonyl compounds, these reactions still find a wide utility in organic synthesis. To a large extent, this has to do with the utility of the Wolff rearrangement, and the subsequent addition of nucleophiles to the ketene that results, for the synthesis of cyclopentane and cyclobutane carboxylic acids for the needs of total synthesis [12].
Notably, the α-carbonyl carbenes formed with the decomposition of cyclic diazo monocarbonyl compounds are more inclined to undergo the Wolff rearrangement than their acyclic counterparts, which is supported by quantum chemical calculations [28]. This has to do with the fact that, in acyclic carbenes, the unshared electron pair is stabilized due to the interaction with the orthogonally oriented π* orbital of the carbonyl group. Because cyclic diazo carbonyl compounds are conformationally fixed, such orthogonal orientation of the unshared pair of the resulting carbene and the carbonyl group cannot be achieved. Hence, the latter type of carbenes has a higher reactivity. For cyclic diazo ketones, the Wolff rearrangement has been shown to be more facile under microwave irradiation than under thermal conditions [29]. For the Wolff rearrangement under microwave irradiation, the choice of the solvent plays a crucial role. For instance, 3-diazo camphor microwaveirradiated in benzylamine gives an excellent yield of ketene adducts. Under thermal conditions, the sole product is that of a formal intramolecular insertion into the C-H bond. However, attempts to bring about the Wolff rearrangement in an aqueous medium does not lead to the formation of the respective carboxylic acid, even under microwave irradiation, since the intramolecular C-H insertion product is the sole one in this case. This has to do with the high absorption of the microwave irradiation by water (due to its high dipole moment) and the resulting heating of the reaction mixture. The said carboxylic acid can only be obtained from 3-diazo camphor under photochemical conditions in 1,4-dioxane (Scheme 8) [29].
Notably, a nucleophile addition to cyclic ketenes tends to proceed with endoselectivity [30][31][32]. The Wolff rearrangement of α-diazo cyclopentanones has found broad applications in organic synthesis. In aqueous tetrahydrofuran or 1,4-dioxane, free cyclobutanecarboxylic acids can be obtained [11,33]. For example, in the total synthesis of ent- [3]-ladderanol, the third cyclobutene ring is introduced in key intermediate 12 through the Wolff rearrangement of the fairly complex α-diazo cyclopentane precursor 13 (Scheme 9). The low diastereoselectivity of the process does not present an issue because the carboxylic acid group is removed in the next step under acidic conditions [11]. Scheme 9. The key step in the synthesis of ent- [3]ladderanol.
The Wolff rearrangement of carbonyl carbenes formed from α-diazo cyclohexanones has gained prominence in organic synthesis; however, it is less widespread compared to their five-membered counterparts. For instance, the photochemical decomposition of diazo compound 18 in wet tetrahydrofuran delivers the respective cyclopentane carboxylic acids 19 (Scheme 12) [40]. Alkyl cyclopentane carboxylate 20 is obtained in the course of the photochemical [30,41] decomposition of bicyclic diazocyclohexane 21 in the presence of methanol, usually employed as a solvent (Scheme 13). Using hexamethyldisylazane as a nucleophile with subsequent acidic hydrolysis allows the obtaining of primary amide 22 (Scheme 14) [42]. Notably, the decomposition of α-diazo cyclohexanones in the presence of nucleophiles typically proceeds diastereoselectively [10,13].
Recently, an enantioselective version of a nucleophile addition to ketenes has been reported. The resulting 8-acylamino isoquinolines 23 were obtained with ee values exceeding 70% (Scheme 15) [43]. One of the enantioenriched building blocks obtained that way (23a) was employed in the total synthesis of (+)-psiguadial B (24) (Scheme 16). The decomposition of cyclic diazo ketones with a subsequent Wolff rearrangement can be employed, not only in total synthesis, but also for the construction of polycyclic cage structures. For instance, the photochemical transformation of bis-diazo cyclohexanone 25 into bis-methyl cyclopentanoate 26 is the key step in the synthesis of iso[1.1.1.1]pagodane 27 (Scheme 17) [44]. The photolysis of the α-diazo cyclopentanone moiety in methanol was successfully employed toward the construction of [4.4.4.5]fenestrane skeleton (28) [40]. Other authors have managed to conduct that reaction diastereoselectively (Scheme 18) [8]. Another application of the photolysis of cyclic diazo monocarbonyl compounds is in the synthesis of the Dewar arenes. In this synthesis, the resulting bicyclohexenecarboxylic ester 29 is selenylated and oxidized with m-CPBA (Scheme 19) [35,45]. The reactions of cyclic ketenes with nucleophiles finds an interesting application in the dye chemistry. The diazo derivative of rhodamine obtained from the respective chloroanhydride is, itself, not luminescent, as it exists in the spiro form. However, its photochemical decomposition in methanol results in the formation of two products. The major product 31 results from the Wolff rearrangement and the addition of a methanol molecule, with a subsequent rupture of the cyclobutene cycle, in which an extended conjugate system is formed, and it demonstrates strong fluorescence. The minor product, resulting from a 1,2-aryl shift in carbonyl carbene, does not display luminescent properties (Scheme 20) [46]. Scheme 20. Photochemical production of strongly luminescent rhodamine B derivatives.
The photoactivation of diazo rhodamines finds application in various areas of bioimaging. In nonactivated form, these dyes are not charged and, therefore, can cross the phospholipid membrane of the cell [46][47][48].
Particularly interesting is the mixed rhodamine-fluoresceine sensor 32 for esterases. The phenolic group in 32 is acylated which leads to a non-luminescing photo adduct. In the presence of esterases, 32 is de-acetylated and, upon photolysis and the addition of external nucleophiles, gives a strongly luminescent product (Scheme 21) [49]. The ketene adduct with nucleophiles may turn out to be rather reactive itself and undergo various post-transformations. With the photochemical decomposition of β-diazoα-tetralone 33 in the presence of vinyl ethylene carbonate and chiral palladium catalyst, spirocycle 34 is formed in high yield and ee. According to the proposed mechanism, the ketene interacts with the nucleophilic oxygen atom of alkoxy-η 3 -allyl ligand of Pd(II). The initial adduct, bidentately coordinated to Pd(II), undergoes intramolecular asymmetric allylic alkylation, which leads to the observed product 34 (Scheme 22). It is likely that β-diazo-α-indanone and its seven-membered analog can also undergo a similar transformation [50]. The Wolff-rearrangement-derived ketenes can interact with more than nucleophiles. For instance, ketenes derived from 3-diazochroman-4-one (35) can undergo [2 + 2] cycloaddition with various olefins delivering 6-oxospiro [3.4]octan-1-ones 36 [51]. The presence of the catalyst is necessary to suppress a competition 1,2-alkyl migration, which would lead to 4-benzopyrans 37. Unfortunately, the reaction appears to be limited to 2,2-disubstituted 3-diazochoman-4-ones, as even monosubstituted ones predominantly undergo 1,2-hydride shift, and ketene is not formed (Scheme 23).

Decomposition of Cyclic α-Diazo Ketones Followed by β-Migration
With the decomposition of α-diazocarbonyl compounds, the resulting diazonium salts can be stabilized via the β-to-α migration of substituents. The stability of 3-diazodihydrofuran-3(2H)-ones 39 towards various protic acids was investigated. The compounds were stable in acetic and formic acids; however, in stronger trifluoroacetic acid, products of β-migration 40 were obtained in high yields. The decomposition of the spirocyclic structures gave annelated products 40a-b (Scheme 25) [54]. Mechanistically, the protonation of the diazo group can lead to the formation of the transition state 41. Upon migration, deprotonation gives the observed olefin 40. This mechanism can justify the selectivity for products 39 containing two different aromatic groups. More electron-rich aryls tend to migrate preferentially (Scheme 26) [55]. For β-hydroxy-substituted substrates, 1,2-migration leads to the enol formation (Tiffeneau-Demjanov rearrangement), whose main tautomer is the dicarbonyl compound. For instance, for 3-hydroxy-2-diazoindan-1-ones 42, formed in situ as the result of intramolecular condensation, decomposition with the subsequent migration of the phenyl substituent or a hydrogen atom takes place on catalysis with tin(II) chloride (Scheme 27) [25]. The same transformation can be catalyzed by p-toluenesulfonic acid [55]. The decomposition of α-diazo-β-hydroxyketones with a subsequent Tiffeneau-Demjanov rearrangement can be employed for building cage structures. Bicyclic α-diazo ketones bearing a hydroxy group in β-position relative to the diazo group (such as 43) can be decomposed in the presence of tetracarboxylates of dirhodium. Since both carbon-carbon bonds leading to this hydroxy group can be fragmented, two products (44 and 45) can be formed in varying ratios. It is supposed that the alkyl migration takes place as a concerted process, which is supported by the preserved stereochemistry of the α-carbon atom (Scheme 28) [24].
In the case of γ'-methoxy substitution (as in 46), along with the rearrangement product (47), a substantial amount of intramolecular C-H insertion product 48 is formed, which is indicative of the reaction proceeding through rhodium carbenes. Additional evidence that the catalyst does not act as a Lewis acid is that the reaction is not workable with acidic catalysts (HCl or BF 3 ·Et 2 O), in which case only products 49 of the dehydration of the starting alcohol are formed (Scheme 29) [24].
Since metal carbene is electrophilic in nature, the reactions primarily involve the rupture of the bond bearing higher electrophilic density on it. For instance, the introduction of an ethoxycarbonyl substituent in the γ-position of 1-diazo-7a-hydroxy octahydro-2H-inden-2-one 50 reduces electron b, and only the path a rearrangement product 51 is selectively formed. The selectivity is affected by the cycle size of the α-diazocarbonyl compound. Going from a five-membered cycle (52) to a six-membered cycle (53), the amount of the path b rearrangement product is increased. Due to stereochemical and energetic considerations, the formation of a cyclopentanone ring (54) is more preferred compared to a cyclobutene ring (55) (Scheme 30) [24].
The importance of the information summarized above is underscored by the frequent occurrence of a bicyclo[m.n.1]alkanone scaffold in various natural products [24]. The said transformation was employed in the construction of a welwistatin core (fragment of alkaloids of the bacteria, Hapalosiphon welwitschii and Westiella intricata) [56]. In an endocyclic mode, β-migration, not only of alkyl but also of allylic substituents, occurs. The decomposition of 6-diazocyclohex-2-enones 56 in the presence of silver triflate leads to the formation of a metal carbene undergoing an endocyclic migration, which leads, in turn, to the formation of 5-alkyliden-2-cyclopentenones 57 in high yields and with an exclusively trans-configured double bond. This transformation requires the presence of at least one substituent in position 5 of the starting diazo compound; otherwise, a β-hydride shift overrides the β-allyl migration, which leads to the formation of corresponding phenols 58 in moderate yields (Scheme 31) [57]. The decomposition of 6-diazocyclohex-2-enones with a subsequent endocyclic βmigration have been found to tolerate the presence of bulky substituents in the substrate. As to the electronic properties, slightly better yields have been observed for substrates bearing an electron-donating group in position 5 of the starting diazo compound, which confirms the reaction proceeding via cationic intermediates. This transformation has an undisputed practical significance, as the resulting 5-alkylidene-2-cyclopentenone scaffold is present in many biologically active compounds (Scheme 32) [58,59]. More practical aspects of the described method become apparent in the case of using 6-diazocyclohex-2-enones with a chiral center in position 5 (such as 59), which can easily be synthesized from suitable natural products. With the decomposition of such substrates and a subsequent β-migration, this stereocenter is usually not epimerized, which allows the obtaining of products 60 with high enantiopurity (Scheme 33) [57].

Scheme 33. Example of chirality transfer from diazo substrates 59.
Of special interest is the fragmentation of bicyclic β-hydroxy-α-diazo-γ-silyloxy ketones 61. Their decomposition, catalyzed by Sn(IV) chloride under mild conditions, delivers macrocyclic alkynones 62. The transformation turns out to be sensitive to the ring size bearing the diazo function. Good results have been obtained with α-diazo cyclohexanone templates. Reducing the ring size to five-membered leads to worse results, according to spectroscopic data; however, isolating it is not feasible due to instability. With the fragmentation of the starting material with an α-diazo cycloheptanone moiety, isolation of the product was possible, but with a significantly reduced yield compared to the six-membered counterpart. Unfortunately, synthesis of an α-diazo cyclooctanone fragment-containing substrate is not feasible. Notably, the reaction is also successfully realized for the transisomers of compounds bearing an α-diazo cyclohexanone fragment; however, the yields are generally lower than for the cis counterparts (Scheme 34) [26]. The presence of the silyloxy group is crucial for the reaction to reach completion. Should the γ-position be substituted with a hydroxy group, intermediate 63 would simply turn into a vinyl cation with a subsequent ring expansion due to the 1,2-alkyl migration [61]. In principle, the silyloxy group could be replaced with a donor alkyl substituent; however, this leads to lower product yields [60]. That is why a strongly donating silyloxy group appears crucial for the fragmentative formation of complex macrocyclic systems [26].

Decomposition of Cyclic α-Diazo Ketones in the Presence of Substrates Containing n-Nucleophiles
The reactions of the decomposition of cyclic α-diazo ketones in the presence of substrates containing n-nucleophiles are well-represented in the literature. The simplest case of this sort of transformation are the reactions of the formal insertion of carbenes into a hydrogen-heteroatom bond (X-H). These reactions presumably proceed through an ylide formation, followed by a proton migration (Scheme 36) [2]. The insertion into the O-H bond of alcohols is poorly studied. However, selected literature examples demonstrate that the reaction can be catalyzed by Lewis acids [63,64] as well as transition metal complexes [65]. The insertion into the O-H bond of allylic alcohols is of much interest, as it can be accompanied by a subsequent sigmatropic rearrangement. Under basic conditions, α-allyloxyketones, such as 64, selectively undergo a [2,3]-sigmatropic rearrangement to give α-allyl-α-hydroxy ketones, such as 65 [63,66]. Alternatively, a [3,3]-sigmatropic rearrangement (66→67) proceeds spontaneously [15] or with thermolysis (Scheme 38) [23,66].

Scheme 38. Allylic O-H insertions accompanied by sigmatropic rearrangements.
The onium ylide formed in the course of the catalytic decomposition of cyclic diazo ketones can be stabilized, not only due to proton migration, but also as the result of an external electrophile addition. A fluorine or trifluoromethyl group bound to hypervalent iodine can act as such an intercepting electrophile (Scheme 39) [67]. Moreover, α-diazoindanone, among other diazocarbonyl compounds, reacts with benzyl alcohol in the presence of an electrophilic SCF 3 source to give the respective α,αbifunctionalized indane 67 (Scheme 40) [68]. The N-H insertions of cyclic α-diazo ketones is well-known. However, as such, without subsequent post-transformations, only one example is known (the reaction of β-diazo-α-tetralone and tert-butylamine) [72]. Much more intriguing are those reactions that involve amines containing an electrophilic moiety in its structure. For example, the product of the Cu(II)-catalyzed reaction of o-alkynyl anilines 68 with cyclic α-diazo ketones 69 immediately undergoes a Michael reaction, giving spirocyclic product 70, which is then fragmented and recyclized with the addition of BF 3 ·OEt 2 . This results in indole derivatives 71, which are valuable precursors en route to natural products (Scheme 43) [73].  Cyclic α-diazo ketones also can participate in a formal chalcogen-halogen bond insertion. The resulting products themselves are of little interest. However, their postmodifications can give rise to difficult-to-access compounds. For instance, the reaction with phenyl sulfenyl chloride with subsequent hydrogen peroxide oxidation gives high yields of α-phenylthio-α,β-unsaturated cyclic carbonyl compounds [75]. Instead of oxidation, the chlorine atom in the initial adducts can be replaced with thiophenol in the presence of Zn(II) chloride to give α,α-bis(arylthio)ketones (Scheme 45) [76]. α-Halo-α-arylselenyl ketones, resulting from the reaction of cyclic α-diazo ketones with phenyl selenyl halides, can also be oxidized. However, in contrast to their sulfurcontaining analogs, this will lead to α-halo-α,β-unsaturated cyclic carbonyl compounds. Unsaturated compounds can be obtained with the PhSe group intact, with treatment with sodium carbonate on the products of formal insertion into PhSeCl (Scheme 46) [77,78].

Reactions of Cyclic α-Diazo Ketones Not Involving Nitrogen Elimination
The simplest case of this type of reaction of cyclic α-diazo ketones is the Staudinger reaction reported for 4-diazotetrahydrofuran-3-ones 76. The reaction is a fast one and gives phosphazines 77 in good yields. The treatment of the latter with aldehydes delivers bis-hydrazones 78 (Scheme 47) [79]. Cyclic α-diazo ketones can act as 1,3-dipoles in cycloaddition reactions with various dipolarophiles, such as electron-deficient acetylenes. The initial spirocyclic adduct 79, formed as the result of a 1,3-dipolar cycloaddition, undergoes subsequent recyclizations as the result of an acyl migration delivering observable pyrazoles 80 (Scheme 48) [80][81][82]. In cases when electron-deficient olefin acts as the dipolarophile, recyclization does not take place [83]. Conformationally more rigid (compared to α-diazo cyclohexanone) α-diazo ketones 88, in reactions with in situ generated benzyne, give spirocyclic intermediates 89, which turn out to be stable at room temperature and are isolated in high yields. They are easily converted into the respective condensed 2H-indazoles 90 in an acidic medium or with simple heating (Scheme 52) [87]. Scheme 52. Dipolar cycloaddition with benzyne of more rigid α-diazo ketones.

2-Diazo-1-indanone was investigated in Rh(II)-catalyzed cyclopropanation reactions.
With cyclohexene, the yields were markedly lower than those obtained with styrene (Scheme 53) [69]. Subsequently, the stereochemical aspects of 2-diazo-1-indanone behavior in Rh(II)catalyzed cyclopropanation reactions with various styrenes were investigated in detail. It was established that, in most cases, the major diastereomer formed has the aryl group in trans-orientation to the carbonyl group, while the reaction is practically insensitive to the steric bulk of that substituent. It was proposed that the underlying reason for such diastereoselectivity is in the stabilization by the carbonyl group of the partial positive charge in the benzylic position (Scheme 54) [88]. 3-Diazochroman-4-ones 91 (along with 2-diazoindan-1-one and β-diazo-α-tetralone) undergo a cyclopropenation reaction with various terminal acetylenes, catalyzed by dirhodium tetraoctanoate delivering spirocyclopropenes 92. The latter can easily be converted into tricyclic furans as a result of recyclization. If BF 3 ·OEt 2 is used as the catalyst, 2-substitutes furans 93 are selectively formed, while using Cu(II) triflate as the catalyst predominantly leads to 3-substituted counterparts 94 (Scheme 55) [89]. Cyclic α-diazo ketones can undergo Pd-catalyzed oxidative cross-coupling reactions with arylboronic acids to give α-aryl-α,β-unsaturated carbonyl compounds 95. Although in general such a transformation is well-studied, for cyclic diazo compounds, there are only a handful of examples in the literature [90][91][92]. Instead of arylboronic acids, only without an oxidant, iodoarenes can be used in similar cross-couplings [91]. Mechanistically, the reaction involves the formation of palladium carbene species 96. Upon migration, within the latter, of the aryl group to the electrophilic carbene carbon atom, β-hydride elimination delivers the observable coupling product 95 (Scheme 56).
Oxidative cross-coupling with α-diazo ketones has been described also for vinyl boronic acids. The transformation has been studied in much detail for a wide range of cyclic α-diazocarbonyl compounds (cyclic α-diazo ketones as well as α-diazo lactones). The reaction demonstrates excellent yields for diazo substrates with more than five atoms in the cycle. With α-diazo cyclopentanone, the yield is a mere 32%. α-Diazo dodecanone is also a competent participant in the reaction. The yield in this case is high, and a sole stereoisomer is obtained; however, the configuration of the double bond has not been established. The same reaction is successful for vinyl boronic acids bearing both aryl and alkyl substituents in the α-position. α-Substituted vinyl boronic acids give much lower yields. The reaction was studied only for trans-configured vinyl boronic acids, and the same configuration of the double bond is preserved in the coupling products (Scheme 57) [93]. α-Diazo cyclohexanone could be arylated with triphenyl boroxine in the presence of a base to give α-phenyl cyclohexanone (Scheme 58) [94]. Scheme 58. α-Arylation with triphenyl boroxine.
As was stated above, cyclic α-diazocarbonyl compounds can be arylated by iodoarenes under oxidative cross-coupling conditions. Such a reaction applied to 6-diazocyclohex-2-enone 97 formally gives 2-aryl cyclohexa-2,5-dien-1-ones 98, which are, essentially, tautomers of the respective arylphenols 99. A wide scope of diazo cyclohex-5-enones and iodoarenes was studied in this context. The reaction turns out to tolerate both electron-donating and electron-withdrawing substituents in the arylating agent; moreover, o-substituted iodoarenes also work very well in this reaction (Scheme 59) [95]. An important aspect of this reaction is that it allows the transfer of chiral information from stereocenters to axially chiral systems. Readily available L-(−)-carvone delivers products with a relatively high enantiopurity with respect to the axis chirality. Replacing the 2-propenyl group with a more sterically demanding isopropyl group in the starting material leads to an increase in both the yield and the enantiomeric purity. Such an approach to enantioselective synthesis of chiral biphenyls holds great promise for the practical synthesis of chiral phosphine ligands and phosphoric acids widely used in enantioselective catalysis (Scheme 61) [95]. The arylation of 6-diazocyclohex-2-enones can be used for the synthesis of dibenzofurans. In this case, the arylating agents must be various o-haloiodoarenes. Once the initial arylation/aromatization is complete, Cu(I) oxide is added into the reaction mixture, and the temperature is raised, which triggers an intramolecular Ullmann reaction. Sometimes, the intramolecular phenol arylation proceeds without any catalyst, albeit in much lower yields (Scheme 62) [96].

Scheme 62. Dibenzofuran synthesis via arylation/aromatization cascade followed by intramolecular Ullmann reaction.
A rather elegant way of synthesizing biphenols from 6-diazocyclohex-2-enones involves C-H functionalization. As the precursors of the second phenol ring, one can use N-aryloxyacetamides. The target biphenols are obtained in high yields in the presence of a Rh(III) catalyst and cesium carbonate. The mild conditions allow the building of the biphenol moiety within a range of biologically active compounds. To get to a chiral biphenol, an L-(−)-carvone diazo derivative is used, as described above. The resulting product with N-β-naphthoxyacetamide is obtained in a low yield but with excellent enantiopurity (Scheme 63) [97]. The following plausible mechanism was proposed for the described biphenol synthesis. N-Aryloxyacetamide initially coordinates to the Rh(III) atom, with a subsequent C-H activation and the formation of cyclometallated complex 101. The latter, upon interaction with the diazo compound, forms a rhodium carbene that undergoes a migratory insertion, forming a second metallocycle (102). β-Hydride elimination, aromatization and reductive elimination then follow, which result in the opening of the metallocycle, accompanied by the reduction of the metal to Rh(I). Intermediate 103, thus formed, undergoes a redox rearrangement, leading to the regeneration of the catalyst. This process is accompanied by the elimination of the target product and acetamide. Apparently, the substituent in position 5 of the starting diazo compound would be oriented towards the sterically encumbered pentamethyl cyclopentadienyl ligand, which explains the low yield obtained with 6-diazo-5-methylcyclohex-2-enone and the L-(−)-carvone derivative. At the same time, using β-naphthoxyacetamide gives a rather high product yield (Scheme 64) [97]. o-Anilino-substituted phenols can be obtained as the result of a cascade oxidative aromatization of the formal N-H insertion products obtained from 6-diazocyclohex-2enones and various amines. o-Arylamino phenols were obtained in a one-pot protocol using Cu(II) acetate in an oxygen atmosphere [98]. It has been proposed that Cu(I) carbenes were at play [99], which decompose with the action of anilines delivering the N-H insertion product. Cu(I) and Cu(II) species catalyze the final step of the oxidative aromatization as the single-electron transfer agents. (Scheme 65) [98]. In the course of N-H insertion, the anilines act as nucleophiles. Hence, with more electron-rich anilines, the reaction gives better yields. The transformation turns out to be sensitive to the steric properties of the anilines and gives lower yields for o-substituted anilines. At the same time, even the presence of a bulky isoprenyl substituent in position 5 of the starting cyclohexanone, does not affect the reaction outcome. The resulting oarylamino phenols are apparent precursors to 1-oxygenated carbazoles, which are present in alkaloids isolated from Rutaceae plants. This is demonstrated by the synthesis of two natural alkaloids-glycozoline and murrayafoline A (Scheme 66) [99]. Later, o-arylamino phenols were synthesized in one-pot fashion using even milder conditions. Using Pd(II) acetate as the catalyst, the reaction was conducted in an open flask. Similar to the copper catalyst, Pd(II) acetate takes part in two catalytic processes: in the formal N-H insertion, it gives a Pd carbene species, and in the oxidative cycle, it transfers electrons.
This method allows the synthesizing of a series of o-arylamino phenols. In this case, all the advantages of the copper-catalyzed method are preserved. However, Pd(II) catalysis allows the involvement of sterically hindered anilines in this reaction without the loss of the yield. For instance, the use of 2,4,6-trimethylaniline gives the target product in 80% yield.
Changing the catalyst to Pd(II) trifluoroacetate also allows good yields with aliphatic amines (including sterically demanding tert-butylamine and diphenylamino methane), which could not be achieved under copper catalysis. Unfortunately, secondary aliphatic amines do not work in these reactions (Scheme 67) [100]. containing an o-fluorophenol moiety, has a significantly higher practical potential, as it more strongly binds to steroid carrier proteins (Scheme 68). The existing synthesis method of this compound does not conform to the demands of radiopharmacology, as the hot fluorine is introduced two steps prior to the completion of its synthesis [101]. Synthesizing 2-[ 18 F]fluoroestradiol through the fluorination of estradiol with electrophilic fluorinating agents is also not an option, as those require the use of 19 F 2 as the career gas, which leads to very low isotopic enrichment. The only drawback of the approach based on the initial difluorination and subsequent HF elimination is the need for the use of an electrophilic fluorinating agent. The low isotope enrichment of the latter results in even lower enrichment of the product. To circumvent this problem, an alternative approach based on halofluorination and subsequent HHal elimination was proposed. Reactions with various electrophilic halogenating agents were screened, and the best results were obtained with N-bromoacetamide (Scheme 71).

Scheme 71. Synthesis of monofluorophenols via bromofluorination.
A serious drawback of this approach, compared to difluorination, is the low yields of the monofluorophenols due to elimination of HF and the formation of numerous sideproducts resulting from electrophilic aromatic bromination. At the same time, when [ 18 F]labeled triethylamine hydrofluoride is used, bromofluorination has one key advantage, namely, the target o-fluorophenol is formed with very high isotope enrichment [102].

Methods of Synthesis
For the first time, α-diazo-γ-butyrolactone was synthesized through formylation and subsequent diazo transfer. Unfortunately, the yield of the target diazo compound was rather low (Scheme 72) [103,104]. Scheme 72. The first synthesis of α-diazo-γ-butyrolactone.

Scheme 75. Oxidation of a hydrazone.
α-Diazo-γ-butyrolactones can be obtained from the respective azide in the presence of a phosphine carrying a succinimide ester function in one of its side chains (such as 106). The mild reaction conditions ensure the tolerance of many functional groups, which make this method, in particular, very suitable for the synthesis of various α-diazo-γ-butyrolactones (Scheme 76) [116]. Six-and seven-membered α-diazo-β-hydroxylactones, as well as their keto-analogs, can be obtained via intramolecular aldol condensation of the suitable terminal diazo esters [60,117].

Decomposition of Cyclic α-Diazo Lactones Followed by β-Migration
α-Diazo-γ-butyrolactones can enter the Büchner-Curtius-Schlotterbeck reaction with cyclic ketones, which results in spirocyclic lactones. In the presence of Lewis acid catalysts, the nucleophilic addition of a diazo lactone to the ketone carbonyl group takes place, followed by the elimination of the nitrogen molecule and Tiffeneau-Demjanov rearrangement. The reaction scope is limited to six-to eight-membered cyclic ketones. Interestingly, when 4-(tert-butyl)cyclohexanone is used as a substrate, the reaction proceeds with high diastereoselectivity. This could be rationalized with the fixation of the cyclohexanone conformation by the sterically demanding substituent and the stereochemical requirements for the a-migration process, accompanied by the nitrogen molecule elimination (Scheme 77) [114]. The decomposition of α-diazo-β-hydroxylactones can be accompanied by a β-alkyl shift that leads to 1,3-dicarbonyl compounds. This transformation has only once been exemplified in the literature in the context of cage-structure synthesis. A Cu(II) triflate catalyzed reaction gave a low yield of the product of decomposition and rearrangement 107 of tricyclic α-diazo-β-hydroxyvalerolactone 108 (Scheme 78) [117]. Similar to the keto-analogs, bicyclic α-diazo-β-hydroxy-γ-silyloxylactones can undergo fragmentation upon the action of Sn(IV) chloride. Unfortunately, for lactones, this transformation is much less effective than for ketones. Similar to ketones, macrocyclic products are obtained with better yields from cis-bicyclic lactones compared to their transcounterparts (Scheme 79) [118].

Decomposition of α-Diazo Lactones in the Presence of Substrates Containing n-Nucleophiles
The first attempts to conduct a formal X-H insertion using α-diazo-γ-butyrolactones were undertaken using Brǿnsted acids as catalysts; however, the target products were obtained with mediocre yields [104].
As to the similar reactions catalyzed by transition metals, it is important to go into the fundamentals of the reactivity of α-diazo lactones. It was established that five-and six-membered α-diazo lactones at low temperature in the presence of a Rh(II) catalyst can undergo a wide spectrum of intramolecular transformations in high yields, even in the case of α-substituted substrates. In particular, within a limited number of examples, it has been shown that β-substituted α-diazo-γ-butyrolactones can enter reactions of formal insertion into S-H, N-H, O-H and Si-H bonds (Scheme 80). The diastereoselectivity of these transformations has not always been high; however, in all cases the trans-isomer was predominantly formed. The trans-isomer content could be increased after the completion of the reaction by epimerizing the reaction mixture in the presence of a base [5]. Scheme 79. Fragmentation of α-diazo-β-hydroxy-γ-silyloxylactones into macrocyclic products. The uniqueness of these transformations is in the fact that the acyclic analogs of α-diazo lactones-α-diazo esters containing a methine group in γ-position-after the formation of the carbene, simply undergo a β-hydride shift, which practically excludes intermolecular reactions. Quantum chemical calculations rationalized this difference in the chemical behavior of α-diazo lactones and α-diazo esters by the different steric properties of the carbenes formed. The carbenes formed from α-diazo esters are stabilized through the interaction with the π* orbital of the carbonyl group, which results in the orthogonal orientation of the carbonyl group and the C-Rh bond. As a result, for steric reasons, the approach of another reacting molecule is blocked, and the carbene finds a way towards stabilization via the β-hydride shift with an olefin formation. In the case of α-diazo lactones, conformational rigidity prevents the orthogonal orientation of the carbonyl group and C-Rh bond, which facilitates any intermolecular reactions (Scheme 81). This hypothesis is supported by the fact that, in contrast to five-and six-membered α-diazo lactones, less rigid α-diazo-β-ethylcaprolactones cannot be involved in intramolecular reactions [5]. Along with Rh(II) carboxylates, the X-H insertion reaction of α-diazo lactones can be catalyzed by gem-containing enzymes. The main advantages of such catalysts are their high enantioselectivity and their high reaction rate. For example, a cytochrome modification was found that turned out to be capable of effectively catalyzing the insertion reaction of α-diazoγ-butyrolactones into aromatic thiols with high enantioselectivity (Scheme 82). Fine-tuning of the enzymes' catalytic properties can be achieved by varying the gem-binding amino acid. In particular, going from cytochrome P411 to cytochrome P450 (essentially, changing from serine to cysteine), the catalytic activity and the enantioselectivity of the catalyzed reaction grows more than five-fold [119].

Scheme 82. Cytochrome-catalyzed S-H insertion reaction of α-diazo-γ-butyrolactones.
Using the cytochrome catalysis, it is possible to obtain B-H insertion products with high enantioselectivity in reactions with boranes and five-and six-membered α-diazo lactones (Scheme 83). Notably, the same reaction with α-diazo caprolactones gives a very low yield. Since the free borane is a reactive compound, unstable in an aqueous medium, its complexes with N-heterocyclic carbenes are used in the reaction. This type of stabilization is dictated by the high biological compatibility of imidazolium salts and their derivatives [110]. In some cases, X-H insertion products derived from α-diazo lactones can be postmodified. For example, the product of a Rh(II)-catalyzed S-H insertion into N-Boc-aminoethanethiol (109) can undergo recyclization into hydroxyethyl-substituted thiomorpholinone 110 (Scheme 84) [120]. The ylide formed in the course of the X-H insertion reaction, instead of undergoing protolytic migration, can find stabilization through the interaction with an electrophile. If both the nucleophilic and electrophilic centers are within the same molecule, the reaction delivers spirocyclic compounds. This is nicely illustrated by the transition metal-catalyzed decomposition of α-diazo-γ-butyrolactones 111 in the presence of 3-hydroxy-and 3-alkylamino ketones 112 (Scheme 85). The diastereoselectivity of the reaction can be rationalized by the fixed ylide conformation due to hydrogen bonding between the amine or alcohol proton and the two carbonyl groups [121,122]. Supposedly, the reaction proceeds through an acetylenide Cu(I) complex that decomposes the diazo lactone, which results in the respective carbene. After the alkynyl migration, the organocopper intermediate formed is alkylated in the presence of the base, delivering the observable final product [113].

Other Reactions of α-Diazo Lactones
Five-and six-membered α-diazo lactones 113-114 react with olefins and terminal acetylenes delivering cyclopropanes and cyclopropenes in high yields. In the case of a substitution in the γ-position of 113-114, the reaction proceeds diastereoselectively. The relative configuration of the chiral center in the β-position strongly depends on the ring size of the starting α-diazo lactone (Scheme 87) [5]. A cyclopropenation reaction of α-diazo-γ-butyrolactones has been reported, even for trimethylsilyl acetylene. In the cyclopropane product 115, the silyl group was removed, and the cyclopropane ring was opened. The resulting α,α-divinyl-γ-butyrolactone 116 served as the key intermediate in the synthesis of (-)-quebrachamine (117) (Scheme 88) [107]. The intramolecular C-H insertion reaction of α-diazo-γ-butyrolactones was studied in detail in connection with its use in the synthesis of furofuranoids. C-H insertion involving the sidechain benzyloxy group of α-diazo-γ-aryl-γ-butyrolactones 121 in the presence of Rh(II) acetate is diastereoselective, in all cases, to give an endo,exo-furofuranone scaffold. This variant of intramolecular C-H insertion was successfully employed in the synthesis of natural furofuranone (±)-epi-aptozimone (Scheme 91) [106]. Later, a convenient method of two-step conversion of the resulting lactones into furans was used, which allowed the synthesizing of a series of natural furofuranone lignanes [105,109,112,124]. Notably, the outcome of these reactions is dependent on the γ-substitution of the starting lactam. For cis-orientation of βand γ-substituents, the yield drops significantly, and a lower diastereoselectivity is observed. This can be rationalized by the destabilizing interactions in the transition state that lead to the endo,exo-product.

Methods of Synthesis of α-Diazo Lactams
Until recently, the only practical method of preparing α-diazo lactams was the nitrozation of the respective α-amino lactams. This approach allowed the preparation of five-and six-membered lactams (exemplified for the six-membered version 125 in Scheme 94) [125,126]. In this case, the synthesis of α-amino lactams is typically conducted from naturally occurring amino acid precursors, which leads to N-unsubstituted α-amino lactams. To access their N-substituted versions 126, alkylation or acylation at the lactam nitrogen atom is typically employed (Scheme 95) [127]. A more common approach to the synthesis of five-membered α-diazo lactams became the so-called Danheiser diazo transfer. Notably, the classical pre-activation of a lactam substrate via trifluoroacetylation had been studied for only one substrate and was not very successful [5]. Later, it was shown that diversely substituted α-diazo-γ-butyrolactams 127 can be accessed via the diazo transfer onto ethoxalylated substrates 128 (Scheme 96) [128]. To purify diazo compounds 127, chromatography on neutral alumina has to be used, since they have been found to be unstable with chromatography on silica, eliminating the nitrogen molecule to give 3-pyrrolen-2-one 128. The latter presumably is formed as the result of the diazo function decomposition and a subsequent 1,2-proton migration. This transformation has been reproduced quantitatively, using only 1 mol% of Lewis acidic silver(I) triflate (Scheme 97) [128]. α-Diazo-γ-lactams bearing alkyl, as well as o-substituted aryl groups on the nitrogen atom, have turned out to be particularly unstable. On standing, they rapidly 'dimerize' (with the extrusion of a nitrogen molecule) into the respective bis-hydrazones 129 (Scheme 98). Greater stability of N-aryl versions (127) can be rationalized by the greater stabilization of the diazo function by the aryl groups due to conjugation. o-Substitution in the aryl group perturbs that conjugation and makes such systems more 'N-alkyl-like' [128]. In order to be able to use such unstable α-diazo-γ-butyrolactams in subsequent transformations, a convenient, one-pot protocol has been developed that does not require the isolation of the diazo compounds in the interim [129].
As a chemical equivalent of NH-α-diazo-γ-butyrolactams, an N-Boc-protected derivative 130 has been developed. Due to the N-Boc group in the precursor 131 being chemically labile, the latter could not be activated by base-promoted acylation. Instead, 131 was activated by α-dimethylaminomethylenation using the Broderick's reagent (132), and such derivative (133) was subjected to a 'SAFE' diazo transfer (Scheme 99) [130]. Scheme 99. Diazo transfer onto N-Boc α-diazo-γ-butyrolactams 131 via α-dimethylaminomethylenation using the Broderick's reagent (132) Just like other diazo compounds, α-diazo lactams can be prepared via the treatment of the respective azido derivatives with a phosphine containing an N-hydroxy succinimide (NHS) group. There seems to be only one example of that strategy applied to an azido compound 134, whereby an α-azido lactam 135 was obtained (Scheme 100). We believe that the scarcity of such examples in the literature has to do with the scarcity of the starting αazido lactams, as well as with the high cost of the NHS-containing phosphine reagent [116].
The O-H insertion reaction of alcohols has been studied well for α-diazo-δ-valerolactams, such as 141. The decomposition of 3-diazopiperidine-2-one (141) in the presence of Rh(II) acetate in an alcohol used as a solvent delivers 3-alkoxypiperidine-2-ones 142 (Scheme 102). The reaction turns out to be sensitive to the sterics of the alcohol reactant-going from methanol to tert-butanol, the yield drops more than 1.5-fold [125]. Later, the reaction of formal insertion into the O-H bond of alcohols and water was studied for α-diazo-γ-butyrolactams [5,128,130]. For the five-membered α-diazo lactams, the transformation turns out to be even more sensitive to the steric bulk of the reacting alcohol. In particular, tert-butanol gives no product at all in this reaction.
α-Diazo-γ-butyrolactams, when decomposed under Rh(II) catalysis, react well in the reaction of the formal S-H insertion (Scheme 103). Interestingly, in contrast to the O-H insertion reaction, this transformation has been found to be less sensitive to the sterical properties of the reacting thiol: even tert-butyl thiol gives a respectable 63% yield in this reaction. This observation can be rationalized by the longer C-S bond in thiols compared to the C-O bond in alcohols [130,132]. A few successful examples of S-H insertion reactions have also been reported for six-membered α-diazo lactams [133]. The S-H insertion reaction of α-diazo-γ-butyrolactams as the means of desymmetrizing symmetrical dithiols (ethane-1,2-dithiol and propane-1,3-dithiol) was later reported as an efficient strategy in constructing novel metallo-β-lactamase inhibitors [134].
Six-and five-membered α-diazo lactams are also capable of entering a formal N-H insertion reaction with aromatic amines under Rh(II) acetate catalysis. The reaction has been shown to be sensitive to the electronic properties of the reacting aniline: the reaction gives better yields with anilines bearing electron-withdrawing substituents. Based on this observation, it has been concluded that the reaction proceeds as a concerted process rather than being mediated by the formation of an ammonium ylide (in which case, more electron-rich anilines would produce better results). It is interesting to note the selectivity of the N-H insertion reaction over O-H insertion: the reaction with o-amino phenol gives absolutely no O-alkylation product. In the case of α-diazo-δ-valerolactams, the N-H insertion reaction is reported not only for anilines but also for such N-H heterocycles as benzotriazole and indole (Scheme 104). Unfortunately, the scope of heterocycles that can be alkylated through such a process is limited. For instance, an attempt to involve imidazole or benzimidazole in this reaction did not even lead to the decomposition of the starting diazo lactam, presumably, due to the poisoning of the Rh(II) catalyst by the coordinating heterocycles. The selectivity of the N-H insertion into external amines and heterocycles over intramolecular N-H insertion into the valerolactams themselves [130,135,136] is also notable in these reactions. 3-Diazopiperidin-2-one can also be chloroselenylated under mild conditions. The initial chloride 143 can be further converted to alkoxide 144, whereupon the phenylselenyl group can be removed under oxidative conditions to give α,β-unsaturated product 145 (Scheme 105) [137]. α-Diazo-δ-valerolactams can be olefinated with aldehydes in the presence of trioxomethyl rhenium and triaryl phosphine (Scheme 106). The diastereoselectivity of the reaction has been shown to be dependent on the structure of the phosphine. The best results are obtained with tris(4-chlorophenyl)phosphine, which gives predominantly (E)configured olefins. Unfortunately, the yields remain rather modest throughout [125,138]. Six-membered α-diazo lactams are also capable of insertion into the C-H bond of indoles and pyrroles under Rh(II) catalysis (Scheme 107). The transformation gives good yields for N-alkyl azoles, while putting an electron-accepting group (acyl or tosyl) on the pyrrole nitrogen atom renders the reaction completely ineffective. This can be rationalized by the reaction proceeding through the formation of a zwitter-ionic intermediate, in which the positive charge is localized on the azole ring [127]. Additionally, the following difference between pyrrole and indole substrates is noteworthy. N-Unsubstituted pyrroles enter the C-alkylation reaction quite readily, while N-unsubstituted indoles primarily give N-H insertion products [127]. Cyclopropanation of α-diazo lactams is featured in the literature only fragmentarily. Six-membered substrates can react with styrenes, enol ethers and dihydrofuran in the presence of Rh(II) acetate [125]. Unfortunately, the reaction is not always diastereoselective. Notably, electron-rich olefins are more readily cyclopropanated, which is illustrated by the formation of a sole enol ether cyclopropanation product 146 in the reaction of a Bocprotected α-diazo-δ-valerolactam with allyl vinyl ether (Scheme 108) [139]. There is only a single example of the cyclopropanation of styrene by a five-membered α-diazo lactam in the literature [5]. α-Diazo-γ-butyrolactams, similarly to α-diazo-γ-butyrolactone, can enter the Büchner-Curtius-Schlotterbeck reaction with cyclic ketones. It has been established that the best results in this reaction can be achieved at a low temperature and by using an equivalent amount of boron trifluoride diethyl etherate as the Lewis acid promoter of the reaction. Interestingly, no spirocyclic product 147 is obtained with Sc(III) triflate as the catalyst, while for α-diazo-γ-butyrolactones, this catalyst works well. Altogether, the reaction works well for six-and seven-membered cyclic ketones but, surprisingly, not for cyclopentanone. Interestingly, when using an N-Boc-protected α-diazo-γ-lactam, the Boc group is removed in the course of the spirocycle formation (Scheme 109) [140]. Scheme 109. The Büchner-Curtius-Schlotterbeck reaction of α-diazo-γ-butyrolactams with cyclic ketones.

Conclusions
As it follows from the material presented above, cyclic α-diazocarbonyl compounds differ from their acyclic counterparts in their chemical properties. The peculiarities of their reactivity have found ample utility in modern synthetic organic chemistry.
At the same time, although different classes of cyclic α-diazocarbonyl compounds are studied equally well and for certain classes, the typical transformations of diazo compounds have been described only fragmentarily in the literature. Specifically, this is true for α-diazo lactones and lactams.
The starting materials for the synthesis of α-diazo lactones are not readily available, which has limited the study of this class of reagents to the simplest, unsubstituted representatives of rather specific examples. Moreover, the chemical transformations of α-diazo lactones described to-date are not particularly diverse, presumably, due to the limited chemical stability of α-diazo lactones themselves.
The situation with α-diazo lactams is more complex and more interesting. Until very recently (2019), the approach to the synthesis of their five-membered variants (α-diazoγ-butyrolactams) was limited to only one, not very advantageous example, which was limiting the study of this class of reagents. At the same time, the chemical stability of available α-diazo-δ-valerolactams was well-established and, hence, a wider range of their chemical transformations has been described in the literature. In contrast, five-membered α-diazo lactams turned out to be much less studied, and this drawback has been addressed only in the last 2-3 years in our laboratories.