Communication Nucleophilic Additions of 2-Furyllithium to Carbonyl Derivatives of L-Serine. Formal Synthesis of (2R,3R)-β-Hydroxy Aspartic Acid ‡

The nucleophilic addition of 2-furyllithium to esters derived from L-serine is described. The obtained furyl ketone 5 is stereoselectively reduced (ds≥95%) with sodium borohydride to afford the corresponding syn aminoalcohol 12 in enantiomerically pure form. Compound 12 was further converted into valuable α-hydroxy-β-amino acids by means of the furan-to-acid equivalence.

Due to the synthetic equivalence of a variety of heterocyclic systems with several functional groups of interest [1], introduction of heterocyclic nuclei into carbon frameworks is the key stage in the synthesis of many biologically active compounds [2].Among the most extensively studied heterocyclic systems are furan [3], benzotriazole [4] and thiazole [5].In particular the furan ring is very attractive because it is resistant to acids and bases but nevertheless is readily cleaved to carboxyl by means of either ruthenium-mediated oxidation or ozonolysis [6].
Reactions of 2-furyllithium 1 with sufficiently active electrophiles, e.g.organic halides, are convenient methods for the formation of a C-C bond [7].Also, the reaction of metalated furans with carbonyl compounds constitutes a useful way of introducing the furan ring; in this context, a vast number of examples concerning the addition of metalated furans to aldehydes and ketones can be found in the literature [8].By contrast, only a few reports on the addition of organometallic derivatives of furan to acid derivatives, such as acid halides, esters or amides have been described [9].In this communication we wish to report our latest efforts at expanding the scope of the synthetic utility of the furan ring.The nucleophilic addition of 2-furyllithium 1 to acid derivatives of L-serine and progress towards α-hydroxy-β-amino acids are discussed.
The starting material of our studies was the O,Ndimethylhydroxamate 4 (Scheme 1) easily available from L-Serine 2 in three steps as described [10].We chose compound 4 since we saw that O,Ndimethylhydroxylamates had been described as suitable electrophiles in nucleophilic additions of organometallic compounds for the synthesis of ketones [11].The addition of 1.05 equivalents of 2-furyllithium 1 to hydroxamate 4 in THF as a solvent afforded the expected furyl ketone 5 in only 20% yield after 12 h at -40 °C, a substantial amount of starting material (c.a.50%) being recovered.Longer reaction times did not improve the conversion and when the reaction was carried out at higher temperatures the yield dropped considerably.It is worth mentioning that Guanti and co-workers reported that compound 4 showed a poor reactivity upon the addition of several organometallic reagents such as ethyl-and vinyllithium [12].
In order to obtain the furyl ketone 5 with an acceptable chemical yield and purity we decided to explore an alternative approach using the well-known methyl ester [13] 6. Two different protecting group arrangements were tried (Scheme 2).Whereas the addition of 2-furyllithium 1 (2.1 equiv., THF, -40 °C) to ester 7 afforded the corresponding ketone 9 in 45% yield, the addition of 1 (1.05 equiv., THF, -40 °C) to ester 8 provided the furyl ketone 5 in 74% yield after 4 h of reaction [14].In both cases a small amount of starting material (c.a.10%) was recovered.If the reaction is extended in order to achieve a higher degree of conversion, the frequent drawback associated with the nucleophilic addition of organometallic reagents to esters (the addition of two molecules of reagent) becomes apparent with the formation of substantial amounts of the tertiary alcohol 11.

COOMe
The furyl ketone 9 can be converted into furyl ketone 5 by replacing the protecting groups, i.e. fluoride-mediated desilylation to afford ketone 10 and subsequent formation of the oxazolidine ring (Scheme 2) Mindful of the highly syn-selective reduction of both α-amino and α-alkoxy ketones with sodium borohydride [15] we decided to exploit that reagent for preparing the required syn aminoalcohol 12.The reduction of 4 was carried out with an excess of NaBH 4 in methanol as solvent at -60 °C and it occurred with an excellent level of diastereoselectivity (ds≥95%), only one isomer being detectable by 1 H NMR spectroscopy (300 MHz) [16].
The almost complete syn selectivity found in the reduction reaction may be ascribed to the Felkin-Anh-Houk open-chain model for asymmetric induction [17] and is also consistent with the earlier observations made regarding the stereoselectivity of the reduction of α-amino ketones [15].Thus the transition state model associated with the reduction of 5 is presented in Figure 1.The application of the furan-to-acid conversion to 12, after protection of the hydroxyl group as an acetate, afforded the carboxylic acid 13 which was converted in situ into the α-hydroxy-β-amino ester 14 [18].The same protocol was applied to 12 after benzoylation of the secondary alcohol thus providing (after in situ benzoylation of the resulting carboxylic acid 15) the known [19] benzyl ester 16.The physical and spectroscopic properties of 16 were in good agreement with those reported for its enantiomer [19].Since the antipode of compound 16 has been previously converted [19] to the enantiomer of the 2-amino-3-hydroxy diamino acid 17, the reaction sequence described above constitutes a formal synthesis of 17, a protected form of the (2R,3R)β-hydroxy aspartic acid [20].
In conclusion, a new approach to syn α-hydroxy-βamino acids via furan chemistry has been achieved.The scope of this methodology and its application to the synthesis of various compounds of interest will be reported in due course.

a
Scheme 1 a

a
Scheme 2 a

Figure 1 .a
Figure 1.Proposed model for the reduction of 5