Regioselective Oxidative Arylation of Indoles Bearing N-Alkyl Protecting Groups: Dual C−H Functionalization via a Concerted Metalation−Deprotonation Mechanism-Reference-Cited by-同舟云学术

Regioselective Oxidative Arylation of Indoles Bearing N-Alkyl Protecting Groups: Dual C−H Functionalization via a Concerted Metalation−Deprotonation Mechanism

Published:2010-09-23 Issue:41 Volume:132 Page:14676-14681
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Potavathri Shathaverdhan¹,Pereira Kyle C.¹,Gorelsky Serge I.¹,Pike Andrew¹,LeBris Alexis P.¹,DeBoef Brenton¹

Affiliation:

1. Department of Chemistry, University of Rhode Island, 51 Lower College Road, Kingston, Rhode Island 02881, and Centre for Catalysis Research and Innovation, Department of Chemistry, University of Ottawa, 10 Marie Curie Pvt., Ottawa, Ontario, Canada K1N 6N5

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja107159b

Reference27 articles.

1. Recent advances in aryl–aryl bond formation by direct arylation

2. Palladium(II)-Catalyzed CH Activation/CC Cross-Coupling Reactions: Versatility and Practicality

3. Transition Metal-Catalysed, Direct and Site-Selective N1-, C2- or C3-Arylation of the Indole Nucleus: 20 Years of Improvements

4. Cross-Dehydrogenative Coupling (CDC): Exploring C−C Bond Formations beyond Functional Group Transformations

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