Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46218
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAgarwal, D D-
dc.contributor.authorJain, R-
dc.contributor.authorRastogi, R-
dc.contributor.authorAgarwal, Vinita-
dc.date.accessioned2019-03-20T05:28:56Z-
dc.date.available2019-03-20T05:28:56Z-
dc.date.issued1992-10-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46218-
dc.description785-787en_US
dc.description.abstractThe epoxidation of cyclohexene gives cyclohexene oxide, cyclohexenol and cyclohexenone as the products. The addition of pyridine as axial ligand promotes the yield. The addition of SLS increases the epoxide yield while addition of Triton-X-100 and CTABr retards the yield. The relative rates of cycloolefin follow the order norbornene > cycloheptene > cyclohexene suggesting that olefin is not coordinated to metal center in the rate determining step.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.31A(10) [October 1992]en_US
dc.titleOlefin epoxidation using iron (III) schiff base complexes as catalysten_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.31A(10) [October 1992]

Files in This Item:
File Description SizeFormat 
IJCA 31A(10) 785-787.pdf88.98 kBAdobe PDFView/Open


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