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Enantioselective synthesis of quaternary α-aminophosphonates by organocatalytic Friedel–Crafts reactions of indoles with cyclicα-ketiminophosphonates 被引量:1
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作者 Zhong Yan Xiang Gao Yong‐Gui Zhou 《Chinese Journal of Catalysis》 CSCD 北大核心 2017年第5期784-792,共9页
An efficient asymmetric Friedel-Crafts reaction has been developed for the synthesis of optically active quaternaryα‐aminophosphonates with up to98%ee.The synthesis involves the reaction of cyclicα‐ketiminophospho... An efficient asymmetric Friedel-Crafts reaction has been developed for the synthesis of optically active quaternaryα‐aminophosphonates with up to98%ee.The synthesis involves the reaction of cyclicα‐ketiminophosphonates with indoles using an H8‐BINOL‐derived chiral phosphoric acid(CPA)catalyst that bears electron‐withdrawing3,5‐ditrifluoromethylphenyl substituents on its3‐and3′‐positions.This Friedel-Crafts reaction of cyclicα‐ketiminophosphonates was also successful with pyrrole. 展开更多
关键词 Friedel–Crafts reaction Quaternary α‐aminophosphonate INDOLE Chiral phosphoric acid
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