Sequential Allylic C–H Amination/Vinylic C–H Arylation: A Strategy for Unnatural Amino Acid Synthesis from α-Olefins-Reference-Cited by-同舟云学术

Sequential Allylic C–H Amination/Vinylic C–H Arylation: A Strategy for Unnatural Amino Acid Synthesis from α-Olefins

Published:2012-02-24 Issue:6 Volume:14 Page:1386-1389
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Jiang Chao¹,Covell Dustin J.¹,Stepan Antonia F.¹,Plummer Mark S.¹,White M. Christina¹

Affiliation:

1. Roger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, Illinois 61801, United States, and Pfizer Worldwide Research & Development, Eastern Point Road, Groton, Connecticut 06340, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol300063t

Reference72 articles.

1. Enantioselective Catalytic Aziridinations and Asymmetric Nitrene Insertions into CH Bonds

2. bEspino, C. G.; DuBois, J.InModern Rhodium-Catalyzed Organic Reactions;Evans, P. A., Ed.Wiley-VCH:Weinheim, 2005; p379.

3. N‐Tosyloxycarbamates as Reagents in Rhodium‐Catalyzed CH Amination Reactions

4. Transition metal catalyzed oxidative functionalization of carbon–hydrogen bonds

5. Aryl−Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation

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