Nickel-Catalyzed Conjugate Addition of Silyl Ketene Imines to In Situ Generated Indol-2-ones: Highly Enantioselective Construction of Vicinal All-Carbon Quaternary Stereocenters-Reference-Cited by-同舟云学术

Nickel-Catalyzed Conjugate Addition of Silyl Ketene Imines to In Situ Generated Indol-2-ones: Highly Enantioselective Construction of Vicinal All-Carbon Quaternary Stereocenters

Published:2017-09-08 Issue:42 Volume:129 Page:13287-13291
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Zheng Jianfeng¹,Lin Lili¹^ORCID,Dai Li¹,Tang Qiong¹,Liu Xiaohua¹^ORCID,Feng Xiaoming¹²^ORCID

Affiliation:

1. Key Laboratory of Green Chemistry & Technology; Ministry of Education; College of Chemistry; Sichuan University; Chengdu 610064 China

2. Collaborative Innovation Center of Chemical Science and Engineering; Tianjin China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Medicine

Reference89 articles.

1. The Anomalous Silico-alkylation of Acetonitrile

2. Oxidative decyanation of arylacetonitriles. Synthesis of ligusticumic acid

3. Silyl Ketene Imines: Highly Versatile Nucleophiles for Catalytic, Asymmetric Synthesis

4. Silylketenimine - vielseitige Nucleophile für die katalytische asymmetrische Synthese

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