doi: 10.1055/s-1996-4177.
A Convenient Synthesis of L-α-Vinylglycine from L-Homoserine Lactone
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- PMID: 29962541
- PMCID: PMC6022833
- DOI: 10.1055/s-1996-4177
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A Convenient Synthesis of L-α-Vinylglycine from L-Homoserine Lactone
Synthesis (Stuttg).
1996 Jan.
Abstract
A procedure for the synthesis of L-α-vinylglycine from L-homoserine lactone is described. The route developed is convenient (only one chromatography step is required) and efficient (72% yield; ≥95% optical yield over 4 steps). Key features include the use of acid-labile protecting groups for the amino (Boc) and carboxyl (diphenylmethyl ester) groups, and the use of the phenylselenolate equivalent derived from sodium borohydride and diphenyl diselenide for L-homoserine lactone cleavage.
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