Palladium-catalyzed 1,2-selective intermolecular arylamination of 1,3-dienes-Reference-Cited by-同舟云学术

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Palladium-catalyzed 1,2-selective intermolecular arylamination of 1,3-dienes

Published:2024 Issue: Volume: Page:
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Li Zhuo-Mei¹,Zhang Zhe¹,Li Xue-Song²,Jiao Rui-Qiang¹,Chen Xi¹,Liu Xue-Yuan¹^ORCID

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry, School of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, P. R. China

2. College of Chemical Engineering, Shenyang University of Chemical Technology, Shenyang 110142, P. R. China

Abstract

This method provides an effective means for the 1,2-selective arylamination of 1,3-dienes, demonstrating a wide substrate scope and excellent functional group tolerance and solving the problem of poor selectivity in dienes.

Funder

National Basic Research Program of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO01365D

Reference65 articles.

1. Synthetic Strategies toward Natural Products Containing Contiguous Stereogenic Quaternary Carbon Atoms

2. Intermolecular Metal-Catalyzed Reductive Coupling of Dienes, Allenes, and Enynes with Carbonyl Compounds and Imines

3. Coordinative Chain Transfer Polymerization

4. Copper-Catalyzed Decarboxylative Functionalization of Conjugated β,γ-Unsaturated Carboxylic Acids

5. Mechanistic approaches to palladium-catalyzed alkene difunctionalization reactions

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