中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Chiral Primary Amine Catalyzed Asymmetric alpha-Benzylation with In Situ Generated ortho-Quinone Methides

文献类型:期刊论文

作者Zhu, Yunbo; Zhang, Wen-Zhao; Zhang, Long; Luo, Sanzhong
刊名CHEMISTRY-A EUROPEAN JOURNAL
出版日期2017
卷号23期号:6页码:1253-1257
关键词Asymmetric Synthesis Chiral Primary Amine Lewis Bases O-quinone Methide B-ketocarbonyls
英文摘要A dual activation strategy integrating primary amine catalysis and Lewis base activation has been developed for an asymmetric alpha-benzylation reaction. Enamines derived from b-ketocarbonyls could react effectively with in situ generated ortho-quinone methides under Lewis base activation in asymmetric alpha-benzylation of beta-ketocarbonyls and a-branched aldehydes. The approach enables the creation of acyclic all-carbon quaternary stereocenters with excellent enantioselectivities and good activity.
语种英语
源URL[http://ir.iccas.ac.cn/handle/121111/38195]  
专题化学研究所_分子识别与功能实验室
作者单位Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
Zhu, Yunbo,Zhang, Wen-Zhao,Zhang, Long,et al. Chiral Primary Amine Catalyzed Asymmetric alpha-Benzylation with In Situ Generated ortho-Quinone Methides[J]. CHEMISTRY-A EUROPEAN JOURNAL,2017,23(6):1253-1257.
APA Zhu, Yunbo,Zhang, Wen-Zhao,Zhang, Long,&Luo, Sanzhong.(2017).Chiral Primary Amine Catalyzed Asymmetric alpha-Benzylation with In Situ Generated ortho-Quinone Methides.CHEMISTRY-A EUROPEAN JOURNAL,23(6),1253-1257.
MLA Zhu, Yunbo,et al."Chiral Primary Amine Catalyzed Asymmetric alpha-Benzylation with In Situ Generated ortho-Quinone Methides".CHEMISTRY-A EUROPEAN JOURNAL 23.6(2017):1253-1257.

入库方式: OAI收割

来源:化学研究所

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