Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/7360
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dc.contributor.authorKumar, Rupesh-
dc.contributor.authorYusuf, Mohamad-
dc.date.accessioned2010-02-15T10:05:22Z-
dc.date.available2010-02-15T10:05:22Z-
dc.date.issued2010-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/7360-
dc.description216-223en_US
dc.description.abstractThe photoirradiation of bischromones with trans-2-butenyl and 2-butynyl, has produced tetracyclic compounds and isomerized ethers as photoproducts. The formation of these photoproducts has been rationalized through H-abstraction by C=O group of the pyrone moiety. The chemical efficiency of the bischromone phototransformations is dictated by the nature of the intermediate spacer unit.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJC-B Vol.49B(02) [February 2010]en_US
dc.subjectPhotoisomerizationen_US
dc.subjectbischromonesen_US
dc.subjectchromophoreen_US
dc.subjectspacer uniten_US
dc.subjectphotocyclisationen_US
dc.titleSynthesis and photochemical H-abstractions of some 2-thienyl/furyl-3-allyloxybischromonesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.49B(02) [February 2010]

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