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Stereoselective synthesis of (2s,3s,4r)-4-amino-3-hydroxy-2-methyl-pentanoic acid,an amino acid constituent of bleomycin,by aldold condensation)
Authors:Masatoshi Narita  Masami Otsuka  Susumu Kobayashi  Masaji Ohno  Yoji Umezawa  Hajime Morishima  Sei-ichi Saito  Tomohisa Takita  Hamao Umezawa
Institution:Faculty of Pharmaceutical Sciences, University of Tokyo Bunkyo-ku, Tokyo 113, Japan;Institute of Microbial Chemistry Shinagawa-ku, Tokyo 141, Japan
Abstract:(2S,3S,4R)-4-Amino-3-hydroxy-2-methylpentanoic acid, a novel amino acid constituent of bleomycin, has been synthesized stereoselectively through aldol condensation of (R)-2-aminopropionaldehyde derivatives and E-vinyloxyboranes.
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