Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/31364
Title: Sulfur-sulfur bond formation through cyclo condensation: Synthesis of some N-glucosylated dithiadiazines
Authors: Ulhe, A G
Chavan, S A
Berad, B N
Keywords: Dithiadiazines;Chloromethane sulfenyl chloride;Glucopyranosyl;Isothiocyanate;Thiosemicarbazides;Sulfur-sulfur bond
Issue Date: Apr-2015
Publisher: NISCAIR-CSIR, India
Abstract: N-Glucosylated 1,2,4,5-dithiadiazines 5 have been synthesized by two different routes which involve the cyclo condensation of thiosemicarbazide and alkyl/arylimino chloromethane sulfenyl chloride. The first route involves the interaction of 4-tetra-O-acetyl-β-d-glucopyranosyl thiosemicarbazide and arylimino chloromethane sulfenyl chlorides while the other route involves the interaction of 4-aryl thiosemicarbazides and N-tetra-O-acetyl-β-d-glucopyranosylimino chloromethane sulfenyl chloride. This cyclo condensation results in sulfur-sulfur bond formation for which very few methods are available. The structures of the newly synthesized 1,2,4,5-dithiadiazines 5 have been confirmed on the basis of certain chemical transformations, IR, 1H and 13C NMR and mass spectral analyses.
Page(s): 570-574
URI: http://hdl.handle.net/123456789/31364
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.54B(04) [April 2015]

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