Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21057
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGoyal, Sunita-
dc.contributor.authorSingh, Anirudh-
dc.date.accessioned2013-09-06T09:17:33Z-
dc.date.available2013-09-06T09:17:33Z-
dc.date.issued2001-06-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21057-
dc.description638-641en_US
dc.description.abstractReactions in 1:1 molar ratio of 2-isopropoxy-4, 4, 5, 5-tetramethyl-1,3, 2-dioxaborolane with N-arylsali-cylaldimines (LH=HOC6 H4CH=NC6H5, HOC6 H4CH =NC6H4Me2-2,6, HOC6H4 CH=NC6H2Me3-2,4,6, HOC6H4CH=NC6H3Et2-2, 6, and HOC6H4CH=NC6H3Pri2-2, 6 in benzene afford new cyclic compounds of boron containing pinacolate and salicylaldiminate groups. These new derivatives have been characterized by elemental analysis and spectroscopic [IR, NMR (1H, 13C, and 11B)] studies as well as by molecular weight determinations.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-A Vol.40A(06) [June 2001]en_US
dc.titleSynthesis and spectral [IR,1H, 13C, and 11B] properties of 2-(N-arylsalicylaldimino)- 4,4,5,5-tetramethyl-1 ,3,2-dioxaborolanesen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.40A(06) [June 2001]

Files in This Item:
File Description SizeFormat 
IJCA 40A(6) 638-641.pdf812.3 kBAdobe PDFView/Open


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