174655-64-2Relevant academic research and scientific papers
A convenient synthesis of L-α-vinylglycine from L-homoserine lactone
Berkowitz, David B.,Smith, Marianne K.
, p. 39 - 41 (1996)
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%; ≥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.
