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A Highly Enantioselective Mannich-Type Reaction of Glycine Schiff Base Catalyzed by a Cinchoninium Salt
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作者 Zhonglin Tao arafate adele +1 位作者 Xiang Wu Liuzhu Gong 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2014年第10期969-973,共5页
A chiral phase-transfer catalyst,derived from the combination of cinchona alkaloid backbone and BINOL skeleton,enabled a Mannich reaction of glycine Schiff base with N-Boc-imines to generateα,β-diamino acid derivati... A chiral phase-transfer catalyst,derived from the combination of cinchona alkaloid backbone and BINOL skeleton,enabled a Mannich reaction of glycine Schiff base with N-Boc-imines to generateα,β-diamino acid derivatives in excellent yields(up to 99%)and with high diastereo-and enantioselectivities(up to>20∶1 dr,96%ee). 展开更多
关键词 phase-transfer catalysis Mannich reaction α β-diamino acid asymmetric catalysis cinchoninium salt
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