Abstract:
A novel method to prepare biologically relevant 1H-imidazol-5(4H)-ones from aliphatic amines, isobutyraldehyde, chloroacetyl chloride and sodium azide under microwave irradiation has been developed.
Citation:
G. P. Kantin, M. Yu. Krasavin, “Microwave-promoted reaction of N-(alk-1-enyl)chloroacetamides with sodium azide unexpectedly yields 1H-imidazol-5(4H)-ones”, Mendeleev Commun., 27:1 (2017), 95–96
Linking options:
https://www.mathnet.ru/eng/mendc1908
https://www.mathnet.ru/eng/mendc/v27/i1/p95
This publication is cited in the following 1 articles:
Maria Chizhova, Dmitry Dar'in, Mikhail Krasavin, “Complications in the Castagnoli-Cushman reaction: An unusual course of reaction between cyclic anhydrides and sterically hindered indolenines”, Tetrahedron Letters, 58:35 (2017), 3470