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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 hydroamidation ; Ni catalysis ; alpha-Acrylamide ; Alkyne ; Aluminum reagent
- Keywords
- ACCESS ; 2-PYRIDONES ; MILNACIPRAN ; ACTIVATION
- 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.
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- Publisher
- Wiley
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