Bacterial Preparation of Enantiopure Unactivated Aziridine-2-carboxamides and Their Transformation into Enantiopure Nonnatural Amino Acids and <i>vic</i>-Diamines
作者:Roberto Morán-Ramallal、Ramón Liz、Vicente Gotor
DOI:10.1021/ol062895b
日期:2007.2.1
by kinetic resolution of their racemates by Rhodococcus rhodochrous IFO 15564 catalyzed hydrolysis. Several regio- and enantioselective nucleophilic ring openings of (1R,2S)-1-benzylaziridine-2-carboxamide or its LAH-reduced product led to a series of enantiopure products, such as O-methyl-l-serine and somevicinal diamines.