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Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3661
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dc.contributor.authorVijay Nair-
dc.contributor.authorBeneesh, P B-
dc.contributor.authorSreekumar, V-
dc.contributor.authorBindu, S-
dc.contributor.authorRajeev S Menon-
dc.contributor.authorAni Deepthi-
dc.date.accessioned2021-02-08T11:57:59Z-
dc.date.available2021-02-08T11:57:59Z-
dc.date.issued2005-
dc.identifier.citationTetrahedron Letters 46(2):201-203; 10 Jan 2005en_US
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/123456789/3661-
dc.description.abstractThe zwitterionic species generated by the addition of dimethoxycarbene to dimethyl butynedioate is trapped by arylidenemalononitrile to yield cyclopentenone derivatives.en_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Scienceen_US
dc.subjectMulticomponent reactionsen_US
dc.subjectDimethoxycarbeneen_US
dc.subjectZwitterionsen_US
dc.subjectCyclopentenoneen_US
dc.titleThe multicomponent reaction of dimethoxycarbene, dimethyl butynedioate and electrophilic styrenes: an unprecedented synthesis of highly substituted cyclopentenone acetalsen_US
dc.typeArticleen_US
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