Primary alkyl bis-catecholato silicates in dual photoredox/nickel catalysis: aryl- and heteroaryl-alkyl cross coupling reactions-Reference-Cited by-同舟云学术

Primary alkyl bis-catecholato silicates in dual photoredox/nickel catalysis: aryl- and heteroaryl-alkyl cross coupling reactions

Published:2016 Issue:4 Volume:3 Page:462-465
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Lévêque Christophe¹²³⁴⁵,Chenneberg Ludwig¹²³⁴⁵,Corcé Vincent¹²³⁴⁵,Goddard Jean-Philippe⁶⁷⁸⁹⁵,Ollivier Cyril¹²³⁴⁵,Fensterbank Louis¹²³⁴⁵

Affiliation:

1. Institut Parisien de Chimie Moléculaire

2. UMR CNRS 8232

3. Sorbonne Universités UPMC Univ Paris 06. 4 Place Jussieu

4. F-75252 Paris Cedex 05

5. France

6. Laboratoire de Chimie Organique et Bioorganique EA 4566

7. Université de Haute-Alsace

8. Ecole Nationale Supérieure de Chimie de Mulhouse. 3 Bis rue Alfred Werner

9. 68093 Mulhouse Cedex

Abstract

Primary alkyl bis-catecholato silicates have been successfully engaged with aryl and heteroaryl bromide substrates in photoredox/nickel dual catalysis to provide cross coupling products.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/QO/C6QO00014B

Reference42 articles.

1. Dual Catalysis Sees the Light: Combining Photoredox with Organo-, Acid, and Transition-Metal Catalysis

2. Merging Visible-Light-Photoredox and Nickel Catalysis

3. Light opens pathways for nickel catalysis

4. Photoredox sheds new light on nickel catalysis: from carbon–carbon to carbon–heteroatom bond formation

5. Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis

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