160708-75-8Relevant academic research and scientific papers
Enantiomerically enriched α-vinyl amino acids via lipase-mediated "reverse transesterification"
Berkowitz, David B.,Pumphrey, James A.,Shen, Quanrong
, p. 8743 - 8746 (2007/10/02)
Reduction of protected α-vinyl amino acids produces "neopentyl" alcohols that may be enriched in the L-antipode by lipase-mediated acylation with vinyl acetate. Subsequent deacetylation, oxidation and hydrolysis yields enantiomerically enriched L-α-vinyl
