Microwave-assisted regioselective synthesis of 2,4-disubstituted imidazoles: Nortopsentin D synthesized by minimal effort

Citation
Pm. Fresneda et al., Microwave-assisted regioselective synthesis of 2,4-disubstituted imidazoles: Nortopsentin D synthesized by minimal effort, SYNLETT, (2), 2001, pp. 218-221
Citations number
31
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
2
Year of publication
2001
Pages
218 - 221
Database
ISI
SICI code
0936-5214(200102):2<218:MRSO2I>2.0.ZU;2-4
Abstract
A two step regioselective synthesis of 2,4-disubstituted imidazoles based o n the reaction of alpha -azidoacetyl indoles with carboxylic acids in the p resence of tertiary phosphines followed by cyclization of the resulting ket oamides by the action of ammonium acetate under microwave irradiation is de scribed. The method has successfully been applied to the synthesis of the a ntifungal nortopsentin D [2,4-bis(3-indolyl)imidazole].