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Catalytic Enantioselective Methanolysis of 4 -substituted-2-phenyl-5(4H)-oxazolones by Cinchonine

Catalytic Enantioselective Methanolysis of 4 -substituted -2-phenyl-5 (4H)-oxazolones by Cinchonine
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摘要 Cinchonine alkaloid catalyzed enantioselective methanolysis of six 4-substituted 2-phenyl-5(4H)-oxazolones to (S)-methyl N-benzoyl-alpha-amino acid esters with 10-33% e.e and 72-81% yield. Cinchonine alkaloid catalyzed enantioselective methanolysis of six 4-substituted 2-phenyl-5(4H)-oxazolones to (S)-methyl N-benzoyl-alpha-amino acid esters with 10-33% e.e and 72-81% yield.
作者 Xie, LJ Hua, WT
机构地区 Beijing Univ
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 1998年第7期605-606,共2页 中国化学快报(英文版)
关键词 CINCHONINE 5(4H)-oxazolone cataytic asymmetric reaction dynamic-kinetic resolution ENANTIOSELECTIVE cinchonine 5(4H)-oxazolone cataytic asymmetric reaction dynamic-kinetic resolution enantioselective
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