Directed copper-catalyzed C–H functionalization of unactivated olefins with azodicarbonamide compounds-Reference-Cited by-同舟云学术

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Directed copper-catalyzed C–H functionalization of unactivated olefins with azodicarbonamide compounds

Published:2024 Issue:38 Volume:14 Page:27475-27480
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Cui Jing¹,Wang Xiaoya¹,Zeng Runsheng¹^ORCID

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P. R. China

Abstract

The copper-catalyzed strategy employing directing group has proven to be a advantageous approach. In this study, we present the successful application of this strategy to accomplish Heck-type coupling reactions and construct β-lactam skeletons.

Funder

Priority Academic Program Development of Jiangsu Higher Education Institutions

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/RA/D4RA04113E

Reference44 articles.

1. Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

2. Transition metal-catalyzed C–H bond functionalizations by the use of diverse directing groups

3. Recent Advances in Metal Catalyzed C−H Functionalization with a Wide Range of Directing Groups

4. Transition-Metal-Catalyzed C–H Bond Activation for the Formation of C–C Bonds in Complex Molecules

5. Recent Development of Regio‐ and Stereoselective Aminohalogenation Reaction of Alkenes

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