Biocatalytical transformations—VI. The 4-acetamido-cyclopent-2-ene carboxylate route revisited: Synthesis of (+)- and (−)-aristeromycin
作者:René Csuk、Petra Dörr
DOI:10.1016/0040-4020(95)00246-5
日期:1995.5
Enantiomerically pure (+)- as well as (−)-aristeromycin can be synthesized starting from (+)- or (−)-butyl (or hexyl) 4-acetamido-cyclopent-2-ene carboxylate; these carboxylates are easily obtained from their corresponding racemates by hydrolysis with the lipase from Candida rugosa.