Reactivity of ynamides with AlCl3 and ICl: Ready access to (E)-α-chloroenamides and (E/Z)-α-chloro-β-iodo-enamides
Author:
Funder
Science and Engineering Research Board
Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
https://link.springer.com/content/pdf/10.1007/s12039-020-01880-4.pdf
Reference61 articles.
1. Selected recent reviews: (a) Dekorver K A, Li H, Lohse A G, Hayashi R, Lu Z, Zhang Y and Hsung R P 2010 Ynamides: A Modern Functional Group for the New Millennium Chem. Rev. 110 5064
2. (b) Evano G, Coste A and Jouvin K 2010 Ynamides: Versatile Tools in Organic Synthesis Angew. Chem., Int. Ed. 49 2840
3. (c) Wang X-N, Yeom H-S, Fang L-C, He S, Ma Z-X, Kedrowski B L and Hsung R P 2014 Ynamides in Ring Forming Transformations Acc. Chem. Res. 47 560
4. (d) Lu T and Hsung R P 2014 Novel ynamide structural analogues and their synthetic transformations Arkivoc i 127
5. (e) Evano G, Jouvin K and Coste A 2013 General Amination Reactions for the Synthesis of Ynamides Synthesis 45 0017
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1. Regio- and Stereocontrolled Hydrohalogenation of Ynamides with N-Halosuccinimides (NXS) as the Halogen Source: Synthesis of (E)-α-Haloenamides;The Journal of Organic Chemistry;2024-01-18
2. α-Haloenamides: Synthesis and Subsequent Transformations;Synthesis;2022-08-09
3. AlCl3-catalyzed regioselective intermolecular α or γ mono- or α,γ bis-hydroalkoxylation of allenamides with alcohols;Organic & Biomolecular Chemistry;2022
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