Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21660
Full metadata record
DC FieldValueLanguage
dc.contributor.authorNadir, U K-
dc.contributor.authorJoshi, Susan-
dc.date.accessioned2013-10-07T10:29:30Z-
dc.date.available2013-10-07T10:29:30Z-
dc.date.issued2003-07-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21660-
dc.description1760-1764en_US
dc.description.abstractReaction of 2-substitutcd N-arylsulphonylaziridines with isothiocyanates using lithium iodide as a catalyst yields iminothiazolidines. Besides the spectral and analytical data, the structure is also confirmed by X-ray crystallographic data.The amount of recovered aziridines decreased by use of DMF and DMSO, instead of acetone, as solvents. The reaction works well also with benzoyl isothiocyanates.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(07) [July 2003]en_US
dc.titleSynthesis of 2-iminothiazolidines through reaction of N-arylsulphonylaziridines with isothiocyanates in the presence of iodide ionsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(07) [July 2003]

Files in This Item:
File Description SizeFormat 
IJCB 42B(7) 1760-1764.pdf905 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.