Efficient preparation of unsymmetrical alkyl–aryl tellurides <i>via</i> a nickel-catalyzed reductive coupling strategy-Reference-Cited by-同舟云学术

Efficient preparation of unsymmetrical alkyl–aryl tellurides via a nickel-catalyzed reductive coupling strategy

Published:2022 Issue:12 Volume:9 Page:3199-3203
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Wang Fei¹,Chen Ying¹,Ackermann Lutz²³^ORCID,Wang Shun-Yi¹^ORCID

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, 199 Ren-Ai Road, Suzhou, Jiangsu 215123, China

2. Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077 Göttingen, Germany

3. Prof. Dr. L. Ackermann Wöhler Research Institute for Sustainable Chemistry, Georg-August-Universität Göttingen, Tammannstraße 2, 37077 Göttingen, Germany

Abstract

A selective cross-coupling between unactivated alkyl bromides and diaryl tellurides through reductive nickel-catalysis is described, which efficiently led to unsymmetrical alkyl–aryl tellurides.

Funder

Priority Academic Program Development of Jiangsu Higher Education Institutions

Soochow University

Deutsche Forschungsgemeinschaft

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO00379A

Reference40 articles.