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作 者:Faqian He Guosong Shen Xiaoyu Yang
机构地区:[1]School of Physical Science and Technology,ShanghaiTech University,Shanghai 201210,China [2]University of Chinese Academy of Sciences,Beijing 100049,China [3]Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China
出 处:《Chinese Journal of Chemistry》2022年第1期15-20,共6页中国化学(英文版)
基 金:NSFC(Grant No.22171186);ShanghaiTech University start-up funding for financial support;the support from Analytical Instrumentation Center(contract no.SPST-AIC10112914),SPST,ShanghaiTech University,and Dr.Na Yu for the X-ray crystallographic analysis.
摘 要:An efficient method for asymmetric synthesis of acyclic α-tertiary amine derivatives has been achieved through enantioselective aminations of α-branched ynones with azodicarboxylates enabled by chiral phosphoric acid catalysis.Moreover,kinetic resolution of racemic starting material was realized under these conditions,which gave access to valuable enantioenriched α-substituted ketones.
关 键 词:Asymmetric catalysis Amination Kinetic resolution Chiral phosphoric acids α-Branched ynones
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