Regioselective Transformations of Unsaturated Systems Catalyzed by Low-Valent Nickel: Cycloaddition, Hydrosilylation, and Dicarbofunctionalization

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Abstract

In this Account, we describe our recent research progress in the development of the functionalization of unsaturated substrates catalyzed by low-valent nickel. In particular, we discuss nickel-catalyzed azide-Alkyne cycloaddition (NiAAC), [2 + 2 + 2] cycloaddition of diynes and nitriles, hydrosilylation of alkynes, and dicarbofunctionalization of 1,3-enynes. Moreover, we highlight our mechanistic studies aimed at elucidating catalytically active nickel intermediates, thereby contributing to the understanding and expansion of nickel-catalyzed synthetic methodologies. 1 Introduction 2 Nickel(0)-Catalyzed Cycloaddition Reactions 3 Nickel(I)-Catalyzed Hydrosilylation and Dicarbofunctionalization Reactions 4 Conclusion and Outlook.

Original languageEnglish
Pages (from-to)1889-1899
Number of pages11
JournalSynlett
Volume36
Issue number13
DOIs
StatePublished - 17 Jun 2025

Bibliographical note

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© 2025. Thieme. All rights reserved.

Keywords

  • cycloaddition
  • dicarbofunctionalization
  • hydrosilylation
  • nickel
  • reaction mechanisms
  • regioselectivity
  • unsaturated systems

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