Photoredox-mediated Minisci C–H alkylation of N-heteroarenes using boronic acids and hypervalent iodine-Reference-Cited by-同舟云学术

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Photoredox-mediated Minisci C–H alkylation of N-heteroarenes using boronic acids and hypervalent iodine

Published:2016 Issue:10 Volume:7 Page:6407-6412
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Li Guo-Xing¹²³⁴⁵,Morales-Rivera Christian A.⁶⁷⁸⁹,Wang Yaxin¹²³⁴⁵,Gao Fang¹²³⁴⁵,He Gang¹²³⁴⁵,Liu Peng⁶⁷⁸⁹,Chen Gong¹²³⁴⁵

Affiliation:

1. State Key Laboratory and Institute of Elemento-Organic Chemistry

2. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)

3. Nankai University

4. Tianjin 300071

5. China

6. Department of Chemistry

7. University of Pittsburgh

8. Pittsburgh

9. USA

Abstract

A photoredox-mediated Minisci C–H alkylation of N-heteroarenes with easily accessible primary and secondary alkyl boronic acids has been developed.

Funder

Nankai University

University of Pittsburgh

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/SC/C6SC02653B

Reference70 articles.

1. Bioactive heterocycles V, Topics in Heterocyclic Chemistry, ed. R. R. Gupta, Springer Verlag, New York, 2008, vol. 11

2. Privileged scaffolds for library design and drug discovery

3. Direct transition metal-catalyzed functionalization of heteroaromatic compounds

4. Transition-Metal-Catalyzed Direct Arylation of (Hetero)Arenes by Cï£¿H Bond Cleavage

5. Innate and Guided C–H Functionalization Logic

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