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dc.contributor.authorGanga, V B-
dc.contributor.authorSuresh, E-
dc.contributor.authorSuresh, C H-
dc.contributor.authorVarma, R Luxmi-
dc.date.accessioned2008-07-29T09:44:11Z-
dc.date.available2008-07-29T09:44:11Z-
dc.date.issued2008-07-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/1754-
dc.description1071-1079en_US
dc.description.abstractThe reactivity of calix[4]bis(spirodienones) depends on the nature of the dienophile used. With 1,4-benzoquinones it acts as a 4π component whereas with 1,2-benzoquinones as a 2π system, yielding benzodioxin derived macrocycles in good yield. Bis(spirodienones) can thus perform as a diene as well as a dienophile in cycloaddition reactions.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.47B(7) [July 2008]en_US
dc.subjectCalix[4]bis(spirodienone)en_US
dc.subjectBenzodioxin derived macrocycleen_US
dc.titleSynthesis of novel heterocyclic calixarenes via the Diels-Alder reaction of calix[4]bis(spirodienones)en_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.47B(07) [July 2008]

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