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Department of Physics and Chemistry
Asymmetric Organic Synthesis and Drug Synthesis Laboratory
1. Journal Articles
Regioselective Transformations of Unsaturated Systems Catalyzed by Low-Valent Nickel: Cycloaddition, Hydrosilylation, and Dicarbofunctionalization
Kim, Gun Ha
;
Jeon, Ji Hwan
;
Jung, Byunghyuck
;
Rohde, Jan-Uwe
;
Hong, Sung You
Department of Physics and Chemistry
Asymmetric Organic Synthesis and Drug Synthesis Laboratory
1. Journal Articles
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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.
URI
https://scholar.dgist.ac.kr/handle/20.500.11750/58586
DOI
10.1055/a-2591-9299
Publisher
Thieme
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Jung, Byunghyuck
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