Synthesis
DOI: 10.1055/a-2567-1329
short review

Transition-Metal-Catalyzed (Ni, Pd) Remote Difunctionalization of Alkenes via Chain-Walking Strategies

Dan Yuan
a   Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, Jiangsu 213164, P. R. of China
,
Chong Liu
b   Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409, USA
,
Fahima Jahan Achal
b   Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409, USA
,
Md Sajib Joardar
b   Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409, USA
,
Ke Yang
a   Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, Jiangsu 213164, P. R. of China
,
Haibo Ge
b   Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409, USA
› Author Affiliations

H.G. acknowledges the Robert A. Welch Foundation and Texas Tech University for financial support. K.Y. acknowledges Changzhou University for financial support.


Abstract

Alkenes are not only crucial feedstocks in the chemical industry but are also extensively present in natural products, pharmaceuticals, and organic functional materials. The direct difunctionalization of alkenes has emerged as a powerful and valuable strategy for the construction of highly functionalized organic skeletons. This short review highlights recent advancements in transition-metal-catalyzed remote 1,n-difunctionalization (n > 2) reactions of alkenes with the focus on innovative strategies involving chain-walking processes to construct complex, highly functionalized organic frameworks.

1 Introduction

2 Nickel Catalysis

3 Palladium Catalysis

4 Conclusion



Publication History

Received: 28 February 2025

Accepted after revision: 26 March 2025

Accepted Manuscript online:
26 March 2025

Article published online:
05 May 2025

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