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Regioselective Transformations of Unsaturated Systems Catalyzed by Low-Valent Nickel: Cycloaddition, Hydrosilylation, and Dicarbofunctionalization
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Title
Regioselective Transformations of Unsaturated Systems Catalyzed by Low-Valent Nickel: Cycloaddition, Hydrosilylation, and Dicarbofunctionalization
Issued Date
2025-08
Citation
Synlett, v.36, no.13, pp.1889 - 1899
Type
Article
Author Keywords
cycloadditionunsaturated systemshydrosilylationdicarbofunctionalizationregioselectivityreaction mechanismsnickel
Keywords
COUPLING REACTIONSTERMINAL ALKYNESC-CAIR1,4-ALKYLARYLATION1,3-ENYNESREACTIVITYCOMPLEXESPALLADIUMAZIDE-ALKYNE CYCLOADDITION
ISSN
0936-5214
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. © 2025. Thieme. All rights reserved.
URI
https://scholar.dgist.ac.kr/handle/20.500.11750/58586
DOI
10.1055/a-2591-9299
Publisher
Thieme
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정병혁
Jung, Byunghyuck정병혁

Department of Physics and Chemistry

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