Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6220
Title: Synthesis of 2-phenylimino-3-aryl-4-S-benzyl-6-hepta-O-acetyl-<img src='/image/spc_char/beta.gif'>-lactosylimino-2,3-dihydro-1,3,5-thiadiazine hydrochlorides
Authors: Tale, P V
Deshmukh, S P
Keywords: 1-Aryl-5-hepta-O-acetyl-<img src='/image/spc_char/beta.gif'>-D-lactosyl-2-S-benzyl-2,4-isodithiobiurets
phenyl isocyanodichloride
<img src='/image/spc_char/beta.gif'>-lactosylimino-1,3,5-thiadiazine
Issue Date: Feb-2006
Publisher: CSIR
Series/Report no.: <b style="">Int</b>.<b style="">Cl</b>.<b style=""><sup>7</sup> C 07 D</b>
Abstract: 2-Phenylimino-3-aryl-4-S-benzyl-6-hepta-O-acetyl-<img src='/image/spc_char/beta.gif'>-lactosyl­imino-2,3-dihydro-1,3,5-thiadiazine hydrochlorides have been prepared by the interaction of 1-aryl-5-hepta-O-acetyl-<img src='/image/spc_char/beta.gif'>-D-lactosyl-2-S-benzyl-2,4-isodithiobiurets and phenyl isocyano­dichloride. The structures of these new N-lactosylated-1,3,5-thiadiazines have been established on the basis of usual chemical transformations and IR, NMR and mass spectral studies.
Description: 558-560
URI: http://hdl.handle.net/123456789/6220
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.45B(02) [February 2006]

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