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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5432
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dc.contributor.authorGoudgaon N.M
dc.contributor.authorShi J
dc.contributor.authorSchinazi R.F.
dc.date.accessioned2020-06-12T15:08:00Z-
dc.date.available2020-06-12T15:08:00Z-
dc.date.issued1998
dc.identifier.citationTetrahedron Letters , Vol. 39 , 14 , p. 1869 - 1872en_US
dc.identifier.uri10.1016/S0040-4039(98)00122-1
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5432-
dc.description.abstractOn thermolysis, o-carboranyl substituted 4-aryl-4- hydroxycyclobutenones 5a-d undergo electrocyclic ring opening followed by ring closure to yield substituted butenolides 6a-d This is in contrast to the thermolysis of cyclobutenones which generally produces substituted quinones.en_US
dc.titleUnexpected formation of novel butenolides by thermolysis of o- carboranyl substituted cyclobutenonesen_US
dc.typeArticle
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