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 Field	Value	Language
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
Appears in Collections:	2005

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