| dc.contributor.author | Chakrabarty, Manas | |
| dc.contributor.author | Kundu, Taraknath | |
| dc.contributor.author | Arima, Shiho | |
| dc.contributor.author | Harigaya, Yoshihiro | |
| dc.date.accessioned | 2013-02-08T11:56:05Z | |
| dc.date.available | 2013-02-08T11:56:05Z | |
| dc.date.issued | 2008-07-07 | |
| dc.identifier | FOR ACCESS / DOWNLOAD PROBLEM -- PLEASE CONTACT LIBRARIAN, BOSE INSTITUTE, akc@bic.boseinst.ernet.in | en_US |
| dc.identifier.citation | Chakrabarty M, Kundu T, Arima S and Harigaya Y (2008) An expedient, regioselective synthesis of novel 2-alkylamino and 2-alkylthiothiazolo[5,4-e]- and-[ 4,5-g]indazoles and their anticancer potential. Tetrahedron 64 (28), 6711-6723. | en_US |
| dc.identifier.issn | 0040-4020 | |
| dc.identifier.uri | 1.Full Text Link -> | en_US |
| dc.identifier.uri | http://ac.els-cdn.com/S0040402008008661/1-s2.0-S0040402008008661-main.pdf?_tid=42bdd01a-71e7-11e2-98c2-00000aacb35f&acdnat=1360325064_593d13a38fa7167753332666b539f586 | en_US |
| dc.identifier.uri | ================================================= | en_US |
| dc.identifier.uri | 2.Scopus : Citation Link -> | en_US |
| dc.identifier.uri | http://www.scopus.com/record/display.url?eid=2-s2.0-45449090774&origin=resultslist&sort=plf-f&src=s&st1=An+expedient%2c&nlo=&nlr=&nls=&sid=728492907C7639E9E6E70CA802473A57.WeLimyRvBMk2ky9SFKc8Q%3a640&sot=b&sdt=sisr&sl=18&s=ALL%28An+expedient%2c%29&ref=%28%28An+expedient%2c+regioselective+synthesis+of+novel%29%29+AND+%28An+expedient%2c+regioselective+synthesis+of+novel+2-alkylamino%29&relpos=21&relpos=1&searchTerm=%28ALL%28An+expedient%2C%29%29+AND+%28%28An+expedient%2C+regioselective+synthesis+of+novel%29%29+AND+%28An+expedient%2C+regioselective+synthesis+of+novel+2-alkylamino%29 | en_US |
| dc.description | DOI: 10.1016/j.tet.2008.05.009 | en_US |
| dc.description.abstract | Several novel 2-alkylamino- and 2-alkylthiothiazolo[5,4-e]- and -[4,5-g]indazoles and their 6-alkyl and 8-alkyl derivatives have been synthesised in high overall yields starting from 5-nitro and 6-nitro-indazoles in a three-step route involving the regioselective cyclisation of thioureidoindazoles and indazolyl dithiocarbamates as the key steps. Some assorted thiazoloindazoles have been screened for anticancer properties, which demonstrated the anticancer potential of at least one product, justifying its further follow-up. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | PERGAMON-ELSEVIER | en_US |
| dc.subject | thiazolo[5,4-e]- and -[4,5-g]indazoles | en_US |
| dc.subject | anticancer | en_US |
| dc.subject | regioselective synthesis | en_US |
| dc.subject | thioureidoindazoles | en_US |
| dc.subject | indazolyl dithiocarbamates | en_US |
| dc.subject | bromine in acetic acid | en_US |
| dc.subject | WOS:000257500500015 | en_US |
| dc.title | An expedient, regioselective synthesis of novel 2-alkylamino- and 2-alkylthiothiazolo[5,4-e]- and -[4,5-g]indazoles and their anticancer potential | en_US |
| dc.title.alternative | TETRAHEDRON | en_US |
| dc.type | Article | en_US |