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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
- cycloaddition ; unsaturated systems ; hydrosilylation ; dicarbofunctionalization ; regioselectivity ; reaction mechanisms ; nickel
- Keywords
- COUPLING REACTIONS ; TERMINAL ALKYNES ; C-C ; AIR ; 1,4-ALKYLARYLATION ; 1,3-ENYNES ; REACTIVITY ; COMPLEXES ; PALLADIUM ; AZIDE-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.
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- Thieme
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