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A stereoselective synthesis of spiro-dioxolanes via the multicomponent reaction of dicarbomethoxycarbene, aldehydes and 1,2-or 1,4-diones

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dc.contributor.author Vijay Nair, G
dc.contributor.author Sindhu Mathai
dc.contributor.author Smitha C Mathew
dc.contributor.author Rath, N P
dc.date.accessioned 2021-02-08T13:45:12Z
dc.date.available 2021-02-08T13:45:12Z
dc.date.issued 2005
dc.identifier.citation Tetrahedron 61(11):2849-2856; 14 Mar 2005 en_US
dc.identifier.issn 0040-4020
dc.identifier.uri http://hdl.handle.net/123456789/3669
dc.description.abstract The three component reaction of acyclic carbonyl ylides generated from dicarbomethoxycarbene and aldehydes with 1,2- and 14-diones is described. The reaction afforded the corresponding spiro-dioxolanes in good yields. en_US
dc.language.iso en en_US
dc.publisher Pergamon-Elsevier Science en_US
dc.subject Dicarbomethoxycarbene en_US
dc.subject Carbonyl ylide en_US
dc.subject Huisgen 1,3-dipolar cycloaddition en_US
dc.subject Spiro-dioxolane en_US
dc.title A stereoselective synthesis of spiro-dioxolanes via the multicomponent reaction of dicarbomethoxycarbene, aldehydes and 1,2-or 1,4-diones en_US
dc.type Article en_US


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