Scope and Mechanism of Allylic C−H Amination of Terminal Alkenes by the Palladium/PhI(OPiv)2Catalyst System: Insights into the Effect of Naphthoquinone-Reference-Cited by-同舟云学术

Scope and Mechanism of Allylic C−H Amination of Terminal Alkenes by the Palladium/PhI(OPiv)2Catalyst System: Insights into the Effect of Naphthoquinone

Published:2010-08-06 Issue:34 Volume:132 Page:11978-11987
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Yin Guoyin¹,Wu Yichen¹,Liu Guosheng¹

Affiliation:

1. State Key Laboratory of Organometallics Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai, China 200032

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja1030936

Reference127 articles.

1. Ring Nitrogen and Key Biomolecules

2. aAndersson, P. G. and Backvall, J.E.In Handbook of Organopalladium Chemistry for Organic Synthesis;Negishi, E., Ed.Wiley-Interscience:New York, 2002; p1859.

3. Recent Advances in Catalytic Intramolecular CH Aminations

4. cJiang, L. and Buchwald, S. L.In Metal-Catalyzed Cross-Coupling Reactions, 2nd ed.Wiley-VCH:Weinheim, 2004; Vol. 2, p699.

5. dHartwig, J. F.In Handbook of Organopalladium Chemistry for Organic Synthesis;Negishi, E., Ed.Wiley-Interscience:NewYork, 2002; p1051.

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