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Regioselective Formal Hydroamidation of Alkynes: Synthesis of α-Substituted Acrylamides
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Title
Regioselective Formal Hydroamidation of Alkynes: Synthesis of α-Substituted Acrylamides
Issued Date
2025-04
Citation
Park, Cheong Hoon. (2025-04). Regioselective Formal Hydroamidation of Alkynes: Synthesis of α-Substituted Acrylamides. European Journal of Organic Chemistry, 28(16). doi: 10.1002/ejoc.202401484
Type
Article
Author Keywords
Formal hydroamidationNi catalysisalpha-AcrylamideAlkyneAluminum reagent
Keywords
ACCESS2-PYRIDONESMILNACIPRANACTIVATION
ISSN
1434-193X
Abstract
The formal hydroamidation of alkyne is a powerful synthetic method that enables the formation of various α,β-unsaturated amides. In this article, the efficient formal hydroamidation of terminal and internal alkynes is described, which constitutes the Ni-catalyzed α-selective hydroalumination of alkynes and subsequent treatment with isocyanates. This method is gram-scalable and the synthetic utility is highlighted by the synthesis of a β-lactam from α-phenyl acrylamide. © 2025 Wiley-VCH GmbH.
URI
http://hdl.handle.net/20.500.11750/58159
DOI
10.1002/ejoc.202401484
Publisher
Wiley
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정병혁
Jung, Byunghyuck정병혁

Department of Physics and Chemistry

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