Recent Advances in Radical-Involved Alkynylation of Unactivated C(sp3)–H Bonds by Hydrogen Atom Abstraction

Author:

Zhang Zheng-Hua12,Wei He1,Li Zhong-Liang3,Liu Xin-Yuan2

Affiliation:

1. School of Chemistry and Chemical Engineering, Linyi University

2. Shenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology

3. Academy for Advanced Interdisciplinary Studies and Department of Chemistry, Southern University of Science and Technology

Abstract

AbstractThe direct C(sp3)–H functionalization is one of the major research topics in synthetic chemistry since C(sp3)–H bonds are ubiquitous in every aspect of chemistry. Despite impressive advances in transition-metal-catalyzed C(sp3)–H activation, the radical-initiated process via hydrogen atom abstraction (HAA) of C(sp3)–H bonds represents a more appealing strategy owing to the mild reaction conditions and good regioselectivity. Given the importance of alkynes as versatile synthons in organic synthesis and key structural motifs in drug discovery, great efforts have been made toward their synthesis via the combination of HAA and alkynylation process in recent years. This review summarizes the recent progress in radical-initiated C(sp3)–H alkynylation reactions with emphasis on the alkynylating reagents and mechanistic discussion.1 Introduction2 Alkynylation of C(sp3)–H via Intermolecular Hydrogen Atom Abstraction3 Alkynylation of C(sp3)–H via Intramolecular Hydrogen Atom Abstraction4 Conclusion

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

SUSTech

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

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