Copper‐Catalyzed Synthesis of gem ‐Bisarylthio Enamines under Redox‐Neutral Conditions-Reference-Cited by-同舟云学术

Copper‐Catalyzed Synthesis of gem ‐Bisarylthio Enamines under Redox‐Neutral Conditions

Published:2019-03-12 Issue:9 Volume:361 Page:2004-2008
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Ni Jiabin¹²,Mao Xiaokang¹³,Zhang Ao¹²⁴

Affiliation:

1. CAS Key Laboratory of Receptor Research, and the State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica (SIMM)Chinese Academy of Sciences Shanghai 201203 People's Republic of China

2. College of PharmacyUniversity of Chinese Academy of Sciences Beijing 100049 People's Republic of China

3. Department of Chemistry, Innovative Drug Research CenterShanghai University Shanghai 200444 People's Republic of China

4. School of Life Science and TechnologyShanghaiTech University Shanghai 201210 People's Republic of China

Funder

Chinese Academy of Sciences

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201900035

Reference49 articles.

1. For selected reviews see:

2. Oxidizing Directing Groups Enable Efficient and Innovative CH Activation Reactions

3. C–C, C–O and C–N bond formation via rhodium(iii)-catalyzed oxidative C–H activation

4. Transition metal-catalyzed C–H functionalization of N-oxyenamine internal oxidants

5. Transition Metal-Catalyzed Reactions Involving Oximes

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