Enantioselective Total Syntheses of (-)-allo-Coronamic Acid, (-)-(Z)-2,3-Methanohomoserine, and (2S,3R)-Cbz-cyclo-Asp-OMe

Article abstract of DOI:10.1016/0957-4166(95)00234-G

The title amino acids have been synthesized in 45, 47, and 63percent overall yields, respectively, from enantiopure aminopentenoates, easily available from D-glyceraldehyde as a source of chirality, following divergent pathways from similar diols as commo