Photo-Induced Cycloaddition Reactions of α-Diketones and Transformations of the Photocycloadducts

Photocycloaddition, along with subsequent transformation of the photocycloadducts, provides expeditious ways to construct various structures. The photo-induced reactions of α-diketones have been reported to proceed via different reaction pathways with the involvement of one or two of the carbonyl groups. Photoinduced reactions of cyclic α-diketones including N-acetylisatin, phenanthrenequinone and isoquinolinetrione with different C=C containing compounds could take place via [2 + 2], [4 + 2] or [4 + 4] photocycloaddition pathways. We have investigated the photoreactions of these cyclic α-diketones with different types of alkenes and alkynes, with a focus on the unusual cascade reactions initiated by the photocycloaddition reactions of these cyclic α-diketones and the applications of these photocycloaddition reactions along with the transformation of the photocycloadducts. In this paper, we discuss the diverse photo-cycloaddition pathways found in the photocycloaddition of o-diones leading to various photocycloadducts and the potential applications of these reactions via further transformation reactions of the adducts.


Introduction
Photo-induced cycloaddition reactions combined with subsequent transformations of the photocycloadducts have played important roles in building diverse organic frameworks [1][2][3][4]. The
In this review we will summarize the photocycloaddition pathways, including [2 + 2], [4 + 2] and [4 + 4] photocycloaddition, found in the reactions of α-diketones, with an emphasis on examples based on our previous work. Various compounds containing C=C or C≡C moieties could react readily with α-diketones upon photo-irradiation and the pathway partition in these photocycloadditions gave different cycloadducts or cascade products. The pathway partitioning depends not only on the nature of the α-diketones, but also on the substituents on the C=C or C≡C moieties. The photocycloadditions of N-acetylisatin with two adjacent carbonyl groups on the indole ring could proceed exclusively via [2 + 2] cycloaddition pathway with simple alkenes or via [4 + 4] cycloaddition pathway with specific oxazoles. Complex photocycloadducts have also been obtained from the [4 + 2] photocycloaddition initiated cascade reactions of N-acetylisatin. Competition of different photocycloaddition pathways has also been observed in the photoreactions of N-acetylisatin. The photocycloadditions of 9,10-phenanthrenequinone showed stronger competition of the [4 + 2] cycloaddition pathway to the [2 + 2] pathway. Besides, [4 + 4] cycloadducts were also found in the reactions of 9,10-phenanthrenequinone with oxazoles. In contrast, the two carbonyl groups in 1,3,4-isoquinolinetriones showed distinct reactivity in photocycloadditions. The C-4 carbonyl group is the common reactive site for photocycloaddition and the C-3 carbonyl group seldom gets involved in photoreactions, except in those with special alkenes such as bicyclopropylidene. Photo-induced cycloadditions of other α-diketones such as di-substituted o-benquinones and benzil via different pathways will also be introduced.
Transformations of photocycloadducts could provide facile ways to construct compounds with highly functionalized structures. Griesbeck et al. have reported that photocycloadditions of carbonyl compounds with oxazoles gave bicyclic oxetanes with highly regio-and diastereoselectivity and hydrolysis of the resulting adducts afforded β-hydroxy-α-amino acid derivatives. We found that hydrolytic cleavage of the bicyclic oxetanes formed by [2 + 2] cycloaddition between 1,3,4-isoquinolinetrione and 5-methoxyoxazoles went through a consecutive transformation to give isoquinolineoxazolines. Moreover, we have developed a facile method to prepare biaryl-fused bislactones using the reaction of [4 + 2] photocycloadducts of phenanthrenequinone with alkenes. The clean and efficient transformations of photocycloadducts from α-diketones will be reviewed in the third part of this paper.

N-Acetylisatin
1H-Indole-2,3-dione (isatin) derivatives have various biological activities [29]. They are basic structural units and important synthetic precursors of many natural alkaloids [30]. With acetylation on the nitrogen atom, N-acetylisatin (IS) becomes a better electron acceptor and shows much higher reactivity in photoreactions than the parent isatin. IS has been found to easily undergo photocycloaddition reactions with a wide range of alkenes [17,21,22], alkynes [18,23] and heterocyclic compounds [20,21,24], and hydrogen abstraction reactions with compounds such as aldehydes [19]. For the two adjacent carbonyl groups on the indole ring, the C3 carbonyl group in IS is more reactive than the C2 amide carbonyl group in photoreactions because the α-alkoxy carbonyl radical is more stable when it is at C3 rather than at C2 [19]. Therefore, all the photoreactions we investigated are initiated at the C3 carbonyl group. However, any subsequent reactions are highly dependent on the structures of the alkenes and may involve the C-3 carbonyl only ([2 + 2] reaction) or involve both C-3 and C-2 carbonyls ( [4 + 2] and [4 + 4] reactions).

[2 + 2] Photocycloadditions Involving IS
Photoreactions of IS with ordinary alkenes or enol ethers are common Paterno-Büchi photocycloadditions with predictable regio-and diastereoselectivities. For example, the reaction of IS with styrene derivatives in benzene took place exclusively via the [2 + 2] pathway and gave the diastereoisomeric spiroxetane products via the nπ* triplet state of IS [22]. The regioselectivity and diastereoselectivity of the reactions depend on the reaction mechanism. In reactions with alkenes of high oxidation potential such as styrenes, the regioselectivity can be rationalized by the frontier molecular orbital (FMO) interactions of the excited IS with the ground state alkene and the formation of the most stable 1,4-diradical intermediate in the reaction. For example, the most stable benzyl 1,4-diradical intermediate A in the photoreaction of IS with styrene led to the formation of 1 and 2 (Scheme 1).

Scheme 1. The photocycloaddition of IS and styrene.
The diastereoselectivity can be accounted for by the "Griesbeck model" [31] of the Salem-Rowland rules [32][33][34][35][36] for intersystem crossing (ISC). Before the intermediary triplet 1,4-diradicals transit to closed-shell products, they must go through ISC to realize spin inversion. The rate of ISC is controlled by spin orbit coupling which depends on the geometries of the diradicals. For the sake of the most effective ISC and C-C bond formation, the axes of the p-orbit of the diradical should be vertical. There are four possible projections leading to trans-or cis-products formation (Figure 1 B-E), while there are also other conformers (such as F) which are suitable for efficient ISC but are not suitable for bond formation because of the long distance between the two radical centers. As for the conformers C and E, there is strong steric hindrance between the phenyl and the carbonyl or phenyl of the isatin framework. Without steric hindrance between phenyl and the isatin framework, B and D are favorable conformers. Compared with B, there is a little steric hindrance in D between the hydrogen atom and the isatin ring. Therefore the formation of the syn-oxetane cycloadduct via B is the most favorable. For the more electron-rich alkenes such as stilbenes with electron-donating substituents, single electron transfer (SET) processes with 3 IS* and ion-radical pair formation are energetically feasible. The regioselectivity of the photocycloaddition is dependent on the charge and spin-density distribution in the ion-radicals [22]. Photoreactions of IS with cyclic or acyclic enol ethers also afforded the bicyclic spiroindoleoxetanes in high yields with high regio-and diastereoselectivity [21]. For example, irradiation of a benzene solution containing IS and benzofuran (λ > 400 nm) gave the two head-to-head isomers 3 and 4 with a ratio of 12:1 (Equation 1 in Scheme 2). Similar reaction between IS and n-butyl vinyl ether afforded head-to-tail product 5 and 6 with preference for the product 5 with syn-configuration (Equation 2 in Scheme 2).

Scheme 2. The photoreactions of IS with enol ethers.
The regio-and stereoselectivity can be explained by the classical 1,4-triplet biradical mechanism without SET involvement. In the photocycloaddition of IS with cyclic enol ethers like benzofuran, the 1,4-diradical intermediate G with a benzyl radical is much more stable than the α-oxygen substituted 1,4-diradical H (Figure 2). Therefore the head-to-head photocycloadducts 3 and 4 were found to be the predominant regioisomers. Meanwhile, a charge density calculation has shown that in the vinyl alkyl ether cation radical, the two vinyl carbon atoms have comparable positive charge density [37], which indicates the 1,4-diradical I with an electon donor is much more stable than J (Figure 2). Therefore the formation of head-to-tail cycloadducts 5 and 6 via I was found to be predominant. The sterically more favorable 1,4-diradical conformers suitable for the efficient ISC and C-C bond formation resulted in the thermodynamically less stable syn-spirooxetanes as the main diastereoisomer. Except for the conventional photoreactions of IS with ordinary alkenes, enol ethers and enol ester, we have also investigated the uncommon photoreactions of IS with strained alkenes and special C=C containing species such as oxazoles. In these photoreactions, the [2 + 2] cycloadducts were formed in competition with other products via different light-initiated pathways which will be reviewed later in this paper. For example, we reported the photoreactions between IS and bicycloalkylidenes including bicyclopropylidene (BCP), cyclopropylidenecyclobutane (CPCB), cyclopropylidenecyclohexane (CPCH) and bicyclohexylidene (BCH) [17]. In these unconventional alkene species with unusual bonding properties [38][39][40][41], the extra strain led to unusual reactivities in their photoreactions with IS. Although spirooxetanes 7-10 derived from the [2 + 2] cycloaddition pathway can be isolated from the reaction mixture ( Figure 3), their overall yields just account for less than 40% of the main products. It is noteworthy that the photoreactions of IS with asymmetric bicycloalkylidenes like CPCB or CPCH gave the regioisomers 8/8i and 9/9i respectively. The formation of 8 or 9 was found to be preferred over that of 8i and 9i, which might be explained by the fact that the steric hindrance for the 1,4-diradical recombination in the former with cyclopropane is less than that in the latter with cyclobutane or cyclohexane. Photocycloadditions of carbonyl compounds with alkynes have not been as extensively explored as those with alkenes. It is known that the Paterno-Büchi reactions of ordinary carbonyl compounds with alkynes usually give α,β-unsaturated carbonyl compounds (the quinone methides) as a result of the spontaneous rearrangements of the thermally labile oxetenes formed by the [2 + 2] cycloaddition [42][43][44][45][46][47][48][49][50]. The electron-withdrawing acetyl group enables IS to react with a variety of alkynes including electron deficient terminal alkynes such as phenylacetylenes or cyclopropylacetylene [18,23] which seldom took part in photocycloadditions with other carbonyl compounds. Photoreaction of IS with 1,2-disubstituted acetylenes also proceeded via the [2 + 2] cycloaddition pathway followed oxetene ring opening to give the β,β-disubstituted 3-alkylideneoxindoles 11 (Scheme 3) [18,23].
On the other hand, photoreactions of IS with terminal alkynes such as phenylacetylenes were found to give complex polycyclic products like the dispiroindole[3,2']furan [3',3'']indole derivatives 12 via a complex tandem reaction course [18,19,23] (Scheme 4). We have investigated the mechanism of this cascade reaction. Firstly, triplet excited IS reacted with phenylacetylene to form quinone methide a. Intermediates b and c were produced via hydrogen abstraction between a and another triplet excited IS. In pathway A, an oxygenphilic attack of the carbonyl radical furnished radical d. An intramolecular radical cyclization in d followed by hydrogen abstraction results in the formation of 12. Alternatively, radical pair b and c may undergo an in-cage radical pair recombination after ISC to give the ketene product f (pathway 2 in Scheme 4).Aldol reaction and isomerization of f gave products 12. Scheme 4. The photoreactions of IS with phenylacetylene.

Photoreaction of IS Initiated by [4 + 2] Cycloaddition
With the two adjacent carbonyl groups, IS could also serve as 4π addend to take part in the higher ordered cycloadditions. The 1,4-diradical intermediate formed between the nπ* triplet excited IS and the alkene has a delocalized spin density, which allows the presence of the 1,6-diradical intermediate. The [4 + 2] cycloadducts of IS with alkenes are usually highly reactive and can react rapidly with another C=O or subject to other fast transformations. In the photoreaction of IS with bicyclohexylidene under inert atmosphere, tiny amount of the [4 + 2] cycloadduct was isolated [17]. Although the yield of the [4 + 2] cycloadduct was as low as 2%, it did provide the direct evidence for the [4 + 2] cycloaddition pathway involved in the photoreaction of IS with strained alkenes.
In the photoreaction of IS with bicyclopropylidene which is highly strained, the [4 + 2] cycloaddition pathway was involved in the formation of two type of final products via the [4 + 2] cycloadduct as intermediate (Scheme 5) [17]. When the reaction was conducted under an inert atmosphere with the least amount of oxygen, the highly reactive C=C in the [4 + 2] photocycloadduct could react with another excited IS via [2 + 2] pathway to give the final [4 + 2 + 2] cycloadducts, which could be obtained as two diastereoisomer 13/14 with a total yield of 10%. Meanwhile, the highly reactive [4 + 2] intermediate could also be photooxygenated under the action of the trace amount of oxygen in the reaction system to afford the oxoisochroman 15 (Scheme 5). It is observed that the formation of 13/14 and 15 seemed to be competitive to each other and a higher concentration of dissolved O 2 favored the formation of 15 [17].
Scheme 5. The photoreactions of IS and BCP.
As shown in Scheme 6, except for the common [2 + 2] photocycloaddition leading to the spirooxetanes, [4 + 4] cycloaddition of the O=C-C=O in IS and the C=C-C=N in oxazoles also happened when the oxazole was properly substituted. Substitution groups on the oxazole showed great influence on the preference of the [2 + 2] or [4 + 4] cycloaddition pathway. For example, the 2,4,5-trimethyloxazole reacted with IS via [2 + 2] cycloaddition pathway exclusively. However, in the reaction of IS with 4-phenyloxazole, the product derived from the [4 + 4] cycloaddition initiated pathway could be isolated with yield up to 97% [24]. The [4 + 4] photocycloadduct was also highly reactive and could react rapidly with another excited IS to give the final [4 + 4]/[2 + 2] product 18. Scheme 6. The photoreactions of IS and oxazoles.
The reason for the dependence of chemoselectivity on the substitution groups on the oxazole ring has been rationalized. The steric hindrance from R 1 group hampers the radical pair recombination in the corresponding 1,7-diradical to give the [4 + 4] cycloaddition intermediate 17 (Scheme 7), while the R 2 group may cause steric hindrance to the 1,4-diradical recombination and therefore disfavors the [2 + 2] cycloaddition to form 16. In accord with this, the 4-aryloxazoles without a substituent R 3 at the C5 atom in the oxazole ring give the [4 + 4] products 18 exclusively. The regio-and diastereoselectivity can also be explained by consideration of the most stable diradicals and the most favorable diradical conformation for the ISC and subsequent C-C bond formation events.

Scheme 7.
The chemo-selectivity in the photoreaction of IS and oxazoles.
We have also investigated the photoreactions of IS with other aza-aryls such as imidazole and thiazole. Compared with oxazoles, both imidazole and thiazoles had much lower reactivity in the photoreaction with IS. The photocycloadducts obtained in these reactions were derived from the [2 + 2] cycloaddition pathway. Our exploration in the photoreactions of IS has demonstrated that IS is a special α-diketone species with diverse transformation pathways in photo-initiated cascade reactions. We are still putting efforts to discover more and more IS-involved photoreactions and found their applications in the synthesis of compounds with biological activities.

Phenanthrenequinone
The photocycloaddition reactions of 9,10-phenanthrenequinone (PQ) as another common α-diketone have been studied by us and others. The photoreactions of PQ with olefins have been known for a long time and its synthetic applications and mechanism have been studied in detail for decades [59][60][61][62]. The photocyloaddition of PQ with C=C usually leads to two types of photocyloadducts, that is, the [2 + 2] keto oxetanes derived from [2 + 2] cycloaddition and the dihydrodioxines from the [4 + 2] cyclo-addition pathway. We will briefly review some of the photocycloadditions of PQ with high chemoselectivity, together with the unusual photocycloadditions happened via [4 + 4] pathway.

[2 + 2] Photocycloaddition of PQ
Photocycloaddition reactions of PQ with alicyclic olefins and bicyclic olefins upon irradiation with visible light (>420 nm) was examined by Maruyama et al. [59]. They found that the reaction of PQ with bicyclic olefins exclusively gave keto oxetanes via the [2 + 2] photocycloaddition pathway (Scheme 8). Other alicyclic olefins gave not only keto oxetanes but also dihydrodioxines and photoreducts. The differences of the chemoselectivity were elucidated in terms of the character of intermediary biradicals. Scheme 8. The photoreaction of PQ and bicyclic olefin.

[4 + 4] Photocycloaddition of PQ
The α-dicarbonyl functionality (O=C-C=O) in PQ could also serve as 4π addend to react with dienes or heterodienes via [4 + 4] cycloaddition [20,24]. In our group, we first reported the [4 + 4] cycloaddition between two heterodienes. Photocycloadditions of PQ and oxazoles gave [4 + 4] products 23 with the 2-azadiene moiety in oxazole as another 4π addend, along with the [4 + 2] cycloadduct 24 and the [2 + 2] cycloadducts 25 (Scheme 10). As we discussed before, the chemo-selectivity in the photoreactions between PQ and oxazoles depend highly on the substitution groups on the oxazoles. The effect of substituents on the oxazole ring on the pathway partitioning in the photocycloaddition of PQ with these oxazoles showed slight differences from that of IS with oxazoles. For example, the reaction of PQ with 2,4,5-trimethyloxazole gave the [4 + 4] photocycloadduct with yields up to 89%. Besides, the [4 + 4] photocycloadduct 23 did not undergo further photocycloaddition. Scheme 10. The photoreactions of PQ and oxazoles.

Isoquinoline-1,3,4-trione
Isoquinolinetriones (IQT) are important biologically active compounds [66,67] and they have been used as building blocks in the synthesis of benzo[c]phenanthridine alkaloids [68,69]. Photoreactivity of IQT was not as high as that of IS or PQ since they could barely react with common alkenes upon photo-irradiation. It also took longer for the total conversion of IQT in their photoreactions with acetylenes or with special C=C containing species such as oxazoles or strained alkenes. In most of these photoreactions of IQT, the C4 carbonyl group on the isoquinoline ring was found to be the only reactive site.

Photoreaction with C=C Containing Species
We have studied the photoreactions between IQT and 2-methyl-5-methoxyoxazoles [27]. The reactions were found to proceed exclusively via a [2 + 2] cycloaddition pathway with excellent chemo-, regio-and diastereoselectivity. The chemoselectivity was much higher than that found in photoreactions of other o-quinones such as IS and PQ [20,24]. The resulting spiroisoquinolineoxetanes 26 were produced with exo-configuration exclusively (Scheme 11). The regioselectivity of the photocycloaddition is determined by the most stable 1,4-diradical intermediate. As shown in Scheme 11, two possible biradical intermediates K and L could be generated in the photocycloaddition of IQT with 2-methyl-5methoxyoxazoles. K is an allylic type radical while L only has an oxygen α to the radical center. Therefore the [2 + 2] cycloaddition proceeded exclusively via K to give the oxetane 26. Scheme 11. The photocycloaddition of IQT with 2-methyl-5-methoxyoxazoles.
The diastereoselectivity can also be explained by the Salem-Rowland rule. There are four possible projections leading to trans-or cis-products formation (Figure 4). There is steric hinderance between C3 carbonyl group of IQT and the R group (N) or between the benzene ring of IQT and the R group (P). The steric hinderance makes the ISC process require much more energy. There is some hinderance between the benzene ring of IQT and the oxazole ring (O), while the steric hinderance in M is the weakest, which makes the yield of the trans-product be higher than that of the cis-product. By far, the only higher order photoreaction of IQT in which both the C3 and the C4 carbonyl groups were involved is the reaction between IQT and the highly strained bicycloalkylidenes. We found that in photo-induced reaction of IQT with CPCB in acetonitrile, three types of products were formed (Scheme 12). Except for the spirooxatane 27 from the [2 + 2] cycloaddition pathway, we also isolated small amounts of the [4 + 2] cycloadduct 28, which is thermally unstable and can be easily converted into 29 upon photoirridiation in the presence of O 2 [17].

Photoreactions with Acetylenes
We have systematically studied the photoreactions of IQT with various acetylenes [26,28]. Compared with IS, IQT showed much lower reactivity in its photoreaction with acetylenes. Therefore photo-irradiation for much longer times was needed to achieve modest conversion of IQT if the acetylene was not substituted by electron-rich groups. For example, in the photoreaction of IQT with phenylacetylene (Equation 1 in Scheme 13), the conversion of IQT was less than 20%, even after 72 hours' irradiation. Electron-rich substitution group linked to the C≡C could greatly accelerate the cascade reaction. Photo-irradiation of IQT with ethoxyphenylacetylene or t-butylphenylacetylene for less than 12 hours could lead to complete conversion of IQT and the formation of the polycyclic products 31 and 32, respectively, in high yields (Equations 2 and 3 in Scheme 13).

Scheme 13. Photoreactions of IQT with differently substituted phenylacetylenes.
In the photoinduced reactions of IQT with diphenylacetylene in acetonitrile, we found that the reaction proceeded smoothly and the product, which precipitated readily from the reaction mixture, was later confirmed to be the dibenz[de,g]-isoquinoline-4,6-dione derivatives 33. The reaction was proposed to proceed via a sequential [2 + 2] photocycloaddition, ring rearrangement of the oxetene and dehydrogenative cyclization, as shown in Scheme 14 [28]. Using the photo-tandem reactions of isoquinolinetrione with acetylenes substituted by different azaaryl rings including pyridine, pyrimidine, pyrazine, and quinoline, we were able to obtain diverse aza-polycyclic frameworks 34-39 with isoquinolinedione fused with naphthalene, quinoline or isoquinoline, quinazoline, and phenanthridine respectively, in yields up to 85% (Scheme 15).

Scheme 15. The photoreaction between IQTs and aryl acetylenes
h v

Scheme 16. The photocycloaddition between o-benzoquinone and ethyl vinyl ether.
The photoreactions of the symmetric α-diketones such as tetrachloro-1,2-benzoquinone with acetylenes have been reported to be highly dependent on the light source. Photoreaction of tetrachloro-1,2-benzoquinone with diphenylacetylene in acetone or acetonitrile irradiated with light of wavelength longer than 400 nm gave the 1:2 adduct 42 via a [4 + 2] cycloaddition pathway (Scheme 17 Equation 1) [75], while two isomeric o-quinomethanes 43 (E-) and 44 (Z-) were formed when o-quinones were irradiated with diphenylacetylene in dichloromethane under 300 nm UV light. Irradiated at 300 nm, the E-isomers could isomerize to the Z-form, but the Z-isomer could not. Novel p-quinomethanes 45 and quinodimethanes 46 (at high concentration) were also formed through the initially produced o-quinomethanes with molecular oxygen (Scheme 17 Equation 2) [49,76].

Acyclic α-Diketones
Photocycloadditions of acyclic o-diones including biacetyl, benzil and 1,2-diketones conjugated with ene-yne have been reported. The photocycloaddition of biacetyl with olefins such as indene, furan, and enol ether gave oxetanes with higher orientational selectivity than in the case of monoketones [78,79]. The photoreaction of biacetyl with electron-deficient olefins did not give cycloadducts, indicating that the excited biacetyl was electrophilic in its reaction with olefins. Besides, the phosphorescence of biacetyl could be quenched by an olefin, indicating that the nπ* triplet state of biacetyl was involved in these reactions. Therefore the reaction mechanism was proposed to be an electrophilic attack of the nπ* triplet state of biacetyl on the olefins to give a biradical intermediate.
It has been reported that photoirradiation of benzil promotes homolytic cleavage of the central C-C bond to generate benzoyl radicals and lead to products like benzoic acid and benzaldehyde [80]. In our work using benzil as the α-diketone to react with oxazoles, [2 + 2] photocycloadducts were obtained as the exclusive photocycloadducts [24]. However, in a recent work using benzil as the 1,2-diketone to react with silyl ketene acetals in benzene solution, production of the [4 + 2] cycloadduct 1,4-dioxene was observed [78].
Photocycloaddition of conjugated -diketones with alkenes has been found to be a clean approach to tetrasubstituted furans (Scheme 18, Equation 1). In the proposed mechanism, the nπ* excited triplet state of the -diketones conjugated with C≡C reacted with alkene to furnish an alkyl propargyl biradical, which further underwent 1,5-closure to give a vinyl carbene. Trapping of the carbene in nonprotic solvents by the adjacent carbonyl group led to the formation of the 2,2'-bifuran derivative 47. The photocyclization of 1,2-diketones conjugated with ene-yne moieties to (2-furyl)carbene was employed as a carbene-generating system. For example, in aprotic solvents the photo-irradiation of the ene-yne conjugated 1,2-diketones which bear a biphenyl system as a carbene trapping unit could initiate tandem cyclizations via a carbene intermediate.

Transformations of Photocycloadducts
The photocycloadducts of α-diketones can be highly reactive and subject to sequential transformations under the same photoreaction conditions. As mentioned above, the [4 + 2] photocycloadducts of IS or IQT with strained alkenes could barely be isolated from the photoreaction mixtures. Transformation of this type of highly reactive photocycloadducts could not be controlled and applied in synthetic chemistry. However, there are moderately reactive photocycloadducts of α-diketones with various alkenes. These photocycloadducts are stable enough to be isolated and purified from the photoreaction mixture. Their transformation under specific conditions thus became controllable and could be developed into useful methods to construct special structural motifs. In this part we will summarize our efforts to develop useful synthetic protocols based on transformations of photocycloadducts of α-diketones.

Transformations of Oxetanes
The [2 + 2] photocycloadditions of cyclic α-diketones with alkenes provide a convenient access to spirooxetanes. The oxetanes are usually acid-or thermolabile products. It is reported that the oxetanes derived from the photoreactions between the carbonyl group in aldehydes or ketones and the double bond in heterocyclic rings such as furans or oxazoles could transform into the corresponding β-hydroxy ketones [82][83][84][85][86][87][88][89]. Griesbeck et al. have developed convenient methods to prepare α-amino-β-hydroxy carboxylic acid derivatives through acid catalyzed hydrolysis of oxetanes derived from photocycloaddition of 5-alkoxyoxazoles with aldehydes [90,91]. The oxetanes derived from α-diketones and alkenes can also undergo acid-mediated transformation reactions. For example, purging dry HCl gas into a solution of 3 derived gave two ring cleavage products 49 and 50 (Scheme 19) and can serve as an efficient approach to indole derivatization at C(3).
In our work using 2-methyl-5-ethoxyoxazole to react with IS under photoirridiation, we observed the formation of two secondary products 52 (31%) and 53 (22%) along with the [4 + 4]/[2 + 2] adduct 51 (12%). The formation of 52 was due to the lability of the corresponding oxetane product in the work-up process under mild acidic conditions, which was similar to that reported by Griesbeck et al. However, the formation of the spirooxazoline product 53 was unusual since it involved the intramolecular cyclization of 52 (Scheme 20) [24]. We then proposed that the acid-mediated transformation of spirooxetanes might involve cascade reactions leading to novel organic frameworks. Therefore we prepared a series of spirooxetanes through the highly regio-and diastereo-selective photocycloaddition of IQT with 2-methyl-5-methoxyoxazoles. The acid-mediated transformation of these spirooxetanes under different acid condition was studied in detail. Scheme 20. The transformation of spiroindoleoxetane derived from IS and 2-methyl-5-ethoxyoxazole.
We found that acid-catalyzed transformation of the spiroisoquinolineoxetanes was highly related to the substituent groups on the oxetane rings as well as the type and amount of acid used. Novel spiroisoquinolineoxazoline products 55 could be obtained upon treatment of the spiroisoquinolineoxetanes with large excess amounts of concentrated HCl or with catalytic amounts of strong organic acids like TFA, MsOH or strong Lewis acids like BF 3 ·Et 2 O and TiCl 4 (Scheme 21) [27]. Bulky substituent groups on the oxetane ring showed favorable steric effects on the transformation from 26 to spiroisoquinolineoxazolines 55. When R was H in 26, the consecutive transformation from 54 to 55 did not happen under mild acidic conditions, but when R was an isopropyl group in 26, the transformation could not stop upon generation of the 54 type product and the spiroisoquinoline-oxazoline type product 55 was the only product obtained. Large excess amount of HCl also favored transformation from 26 to 55. Strong Brönsted acids and Lewis acids could catalyze direct transformation from 26 to 55 efficiently, but via different pathways leading to different ratios of diastereoisomers.
We proposed two reaction pathways to explain the acid-mediated transformation. In pathway A, there was no stereogenic center involved, so the configuration was conserved. In pathway B, the C-O bond between the isoquinoline and the oxetane O underwent bond cleavage, leading to the carbocation as an intermediate. Nucleophilic attack of the carbonyl group to the carbocation could proceed from different directions to give 55 and 55i, respectively. Reaction of 26 catalyzed by different types and amounts of acids proceeded simultaneously and competitively via pathways A and B, which resulted in different ratios of 55 and 55i in the final products (Scheme 22). Meanwhile, the diastereoselectivity of the transformation was highly dependent on the group R. Bulky substituents like benzoyl were apt to form spiroisoquinolineoxazolines with single configuration, while small ones like methyl led to spiroisoquinolineoxazolines with isomers. Based on the photocycloaddition of IQT with 5-methoxyoxazoles and this novel acid-catalyzed transformation of the photocycloadducts, facile syntheses of spiroisoquinolines could be realized. For the spiroisoquinolineoxetanes obtained from photocycloaddition of IQT with, their acid-mediated transformation reactions were found to be adjustable through the type and amount of acid used.

Scheme 22.
Proposed pathway for the formation of 55 and 55i.

Transformations of 1,4-Dioxins
The [4 + 2] photocycloaddition of some -diketone such as PQ and C=C containing species gave 1,4-dioxins which are relatively stable. Therefore the transformation of 1,4-dioxins has rarely been investigated. Recently we developed a facile photochemical approach to biaryl-containing medium-ring bislactones with easily available reactants via a concise photocycloaddition-photooxidation sequence through the 1,4-dioxin intermediate [25]. Starting from PQ or 1,10-phenanthroline-5,6-dione (PN) with C=C-containing compounds, we were able to prepare ten-membered bislactones containing biphenyl or bipyridine in a highly atom-economic way (Scheme 23). The first step in the reaction sequence was the photoinduced [4 + 2] cycloaddition of the dione with the C=C bond to form the dioxinophenanthrene or dioxinophenanthroline. Further transformation of the dioxinophenanthrene or dioxinophenanthroline into the biaryl-containing medium-ring bislactones 56 happened rapidly upon photoirradiation under oxygen atmosphere with yields up to 90%. Scheme 23. The photo-oxygenations of the [4 + 2] cycloadducts between PQ and alkenes.

Conclusions
In this paper we have summarized the photo-induced reactions of α-diketones with C=C or C≡Ccontaining compounds with focus on those that have been the subject of our continued interest in the past decade, namely the photoreactions of three type of α-diketones: IS, PQ and IQT. The photocycloaddition pathways, including [2 + 2], [4 + 2] and [4 + 4] photocycloadditons, were explained in detail with representative examples from our work and others. The photocycloadditions of IS proceed exclusively via a [2 + 2] cycloaddition pathway with simple alkenes or via [4 + 4] cycloaddition pathways with specific oxazole. Complex photocycloadducts have also been obtained from the [4 + 2] photocycloaddition-initiated cascade reactions of IS. The photocycloadditions of PQ showed stronger competition of the [4 + 2] cycloaddition pathway to the [2 + 2] pathway. Besides, [4 + 4] cycloadducts were also found in the reactions of PQ with oxazoles. In contrast, the two carbonyl groups in IQT showed distinct reactivity in photocycloadditions. The C-4 carbonyl group is the common reactive site for photocycloadditions and the C-3 carbonyl group seldom gets involved in photoreactions, except in those with special alkenes such as bicyclopropylidene. The pathway partitioning depends not only on the nature of the α-diketones, but also on the substituent groups on the C=C or C≡C moieties. Chemo-, regio-and stereoselectivity in the photocycloadditions were also rationalized. Transformations of photocycloadducts were also briefly reviewed, since they could provide facile ways to construct compounds with highly functionalized structures.