Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/11407
Title: Iodine-catalysed conjugate addition of indole with <img src='/image/spc_char/alpha.gif' border=0> -cinnamylideneketones: Formation of <img src='/image/spc_char/beta.gif' border=0>-(3-indolyl)-<img src='/image/spc_char/alpha.gif' border=0> ,<img src='/image/spc_char/beta.gif' border=0>-dihydro-<img src='/image/spc_char/alpha.gif' border=0> -cinnamylideneketones and bis(3- indolyl)methylbenzene
Authors: Pal, Rammohan
Mandal, Tapas K
Mallik, Asok K
Keywords: <img src='/image/spc_char/alpha.gif' border=0> -Cinnamylideneketones
Indole
<img src='/image/spc_char/beta.gif' border=0>-(3-indolyl)-<img src='/image/spc_char/alpha.gif' border=0>
<img src='/image/spc_char/beta.gif' border=0>-dihydro-<img src='/image/spc_char/alpha.gif' border=0> -cinnamylideneketones
Bis(3-indolyl)methylbenzene
Molecular iodine
Issue Date: Apr-2011
Publisher: NISCAIR-CSIR, India
Abstract: <img src='/image/spc_char/beta.gif' border=0>-(3-Indolyl)-<img src='/image/spc_char/alpha.gif' border=0> ,<img src='/image/spc_char/beta.gif' border=0>-dihydro-<img src='/image/spc_char/alpha.gif' border=0> -cinnamylideneketones and bis(3-indolyl)methylbenzene have been obtained in moderate to good yield by conjugate addition of indole with <img src='/image/spc_char/alpha.gif' border=0> -cinnamylidene¬≠ketones under mild reaction condition in dry ethanol using iodine as catalyst. The structures of the products have been established from their spectral data.
Description: 619-623
URI: http://hdl.handle.net/123456789/11407
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.50B(04) [April 2011]

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