dc.contributor.author | Parvatkar, P.T. | |
dc.contributor.author | Majik, M.S. | |
dc.date.accessioned | 2015-11-06T05:52:50Z | |
dc.date.available | 2015-11-06T05:52:50Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | RSC Advances, vol.4; 2014; 22481-22486. | |
dc.identifier.uri | http://drs.nio.org/drs/handle/2264/4855 | |
dc.description.abstract | Synthesis of two linear indoloquinolines i.e. 6H-indolo[2,3-b]quinoline & 11-hydroxy-10H-indolo[3,2-b]quinoline, and spiro[2H-indole-2,3'-oxindole] from a common intermediate, (2-nitrophenyl)methylidene-dihydro-indolone derivative is described using microwave-mediated reductive cyclization as the key step. | |
dc.language.iso | en | |
dc.publisher | Royal Society of Chemistry | |
dc.rights | An edited version of this paper was published by and © The Royal Society of Chemistry 2014. http://dx.doi.org/10.1039/c4ra02814g | |
dc.subject | Synthesis | |
dc.subject | cyclization | |
dc.title | Microwave-assisted reductive cyclization: An easy entry to the indoloquinolines and spiro[2H-indole-2,30-oxindole]. | |
dc.type | Journal Article | |