Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/9710
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dc.contributor.authorSingh, M Dhaneshwar-
dc.contributor.authorNingombam, Anjana-
dc.date.accessioned2010-06-08T05:40:28Z-
dc.date.available2010-06-08T05:40:28Z-
dc.date.issued2010-06-
dc.identifier.urihttp://hdl.handle.net/123456789/9710-
dc.description789-794en_US
dc.description.abstract1-Succinimidoanthracene undergoes Diels-Alder  reaction with maleic  anhydride to give mainly the anti adduct suggesting that the steric factors play dominant role in deciding the anti/syn stereoselectivity. 1-phthalimidoanthracene and also gives mainly the anti adduct with maleic anhydride. The configurations of the compounds have been established by preparing the corresponding imide derivatives of the anhydride adducts and observing the interactions between the imide substituent and the 1-substituent.The interactions between the 1-substituent and that on the anhydride ring of the adduct are more or less negligible in the anti-adduct. en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJC-B Vol.49B(06) [June 2010]en_US
dc.subject1-Succinimidoanthraceneen_US
dc.subject1-phthalimidanthraceneen_US
dc.subjectstereoselectivityen_US
dc.subjectanhydride adductsen_US
dc.subjectsteric factorsen_US
dc.titleHigh stereoselectivity in the Diels-Alder reaction of substituted anthracenes: Reactions of 1-succinimidoanthracene and 1-phthalimidoanthracene with maleic anhydrideen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.49B(06) [June 2010]

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