Catalyst-controlled regiodivergent C–H bond alkenylation of 2-pyridylthiophenes-Reference-Cited by-同舟云学术

Catalyst-controlled regiodivergent C–H bond alkenylation of 2-pyridylthiophenes

Published:2023 Issue:57 Volume:59 Page:8842-8845
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhang Qiang¹,Zhou Pengfei¹,Zhao Yaokun¹,Liu Yeran¹,Liang Taoyuan¹^ORCID,Jiang Jun¹^ORCID,Zhang Zhuan¹^ORCID

Affiliation:

1. Guangxi Key Laboratory of Electrochemical Energy Materials, Guangxi Colleges and Universities Key Laboratory of Applied Chemistry Technology and Resource Development, School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, P. R. China

Abstract

A novel and effective RhIII- and PdII-controlled switchable C–H alkenylation of 2-pyridylthiophenes with alkenes is realized.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CC/D3CC02411C

Reference66 articles.

1. The Nitroso Ene Reaction: A Regioselective and Stereoselective Allylic Nitrogen Functionalization of Mechanistic Delight and Synthetic Potential

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4. Catalytic Selective Synthesis

5. The medicinal chemist's toolbox for late stage functionalization of drug-like molecules

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