Please use this identifier to cite or link to this item:
http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4485
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Biradar, JS | |
dc.contributor.author | Sharanbasappa, B | |
dc.date.accessioned | 2020-06-12T15:04:04Z | - |
dc.date.available | 2020-06-12T15:04:04Z | - |
dc.date.issued | 2011 | |
dc.identifier.citation | SYNTHETIC COMMUNICATIONS , Vol. 41 , 6 , p. 885 - 890 | en_US |
dc.identifier.uri | 10.1080/00397911003707071 | |
dc.identifier.uri | http://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.publisher | TAYLOR & FRANCIS INC | |
dc.subject | Benzimidazoles | |
dc.subject | conventional method | |
dc.subject | environmentally benign | |
dc.subject | indole | |
dc.subject | microwave irradiation | |
dc.subject | solid support | |
dc.title | MK-10 Clay-Catalyzed Synthesis of 2-(2',5'-Disubstituted-1'H-indol-3'-yl)-1H-benzo[d]imidazoles under Conventional and Microwave Irradiation | en_US |
dc.type | Article | |
Appears in Collections: | 1. Journal Articles |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.