Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4485
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dc.contributor.authorBiradar, JS
dc.contributor.authorSharanbasappa, B
dc.date.accessioned2020-06-12T15:04:04Z-
dc.date.available2020-06-12T15:04:04Z-
dc.date.issued2011
dc.identifier.citationSYNTHETIC COMMUNICATIONS , Vol. 41 , 6 , p. 885 - 890en_US
dc.identifier.uri10.1080/00397911003707071
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4485-
dc.description.abstract[image omitted] The synthesis of benzimidazoles has been achieved in a one-pot reaction in excellent yield using a newly developed methodology. 2,5-Disubstituted-3-cyanoacetyl indoles were directly condensed with substituted orthophenylenediamine via microwave irradiation under neat, solid support, and conventional conditions in a short time to afford the corresponding products in good yields. Structures of the products thus obtained were confirmed by their melting points, infrared, 1H NMR, 13C NMR, and mass spectral data.en_US
dc.publisherTAYLOR & FRANCIS INC
dc.subjectBenzimidazoles
dc.subjectconventional method
dc.subjectenvironmentally benign
dc.subjectindole
dc.subjectmicrowave irradiation
dc.subjectsolid support
dc.titleMK-10 Clay-Catalyzed Synthesis of 2-(2',5'-Disubstituted-1'H-indol-3'-yl)-1H-benzo[d]imidazoles under Conventional and Microwave Irradiationen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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