Palladium(II)‐Catalyzed Aminotrifluoromethoxylation of Alkenes: Mechanistic Insight into the Effect of N ‐Protecting Groups-Reference-Cited by-同舟云学术

Palladium(II)‐Catalyzed Aminotrifluoromethoxylation of Alkenes: Mechanistic Insight into the Effect of N ‐Protecting Groups

Published:2020-04 Issue:4 Volume:38 Page:346-350
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Chen Chaohuang¹,Hou Chuanqi¹,Chen Pinhong¹,Liu Guosheng¹²

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road Shanghai 200032 China

2. Shanghai Hongkong Joint Laboratory in Chemical Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road Shanghai 200032 China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.201900516

Reference57 articles.

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2. (b)Brunet J. J.;Neibecker D.Catalytic Hydroamination of Unsaturated Carbon‐Carbon Bonds. inCatalytic Hetero‐functionalization Eds.: Togni A.; Grützmacher H Wiley‐VHC New York 2001; pp.91–141;

3. (c)Hong S.;Marks T. J.Organolanthanide‐Catalyzed Hydroamination.Acc. Chem. Res.2004 37 673–686;

4. Palladium Oxidase Catalysis: Selective Oxidation of Organic Chemicals by Direct Dioxygen-Coupled Turnover

5. Catalytic Markovnikov and anti-Markovnikov Functionalization of Alkenes and Alkynes: Recent Developments and Trends

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