Facile Baylis-Hillman reaction of substituted 3-isoxazolecarbaldehydes: The impact of proximal heteroatom within a heterocycle on the acceleration of reaction

Roy, Amrendra K; Batra, Sanjay

dc.contributor.author	Roy, Amrendra K
dc.contributor.author	Batra, Sanjay
dc.date.accessioned	2007-11-15T07:31:13Z
dc.date.available	2007-11-15T07:31:13Z
dc.date.issued	2003
dc.identifier.citation	Synthesis(2003), 2325-2330	en
dc.identifier.uri	http://hdl.handle.net/123456789/26
dc.description.abstract	The fast and facile Baylis-Hillman reaction in substi-tuted 3-isoxazolecarbaldehydes confirms the impact of the proxi-mal heteroatom within a heterocycle towards enhanced reactivity of the formyl group for this reaction	en
dc.format.extent	110654 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CDRI Communication No. 6430	en
dc.subject	Baylis-Hillman reaction	en
dc.subject	3-isoxazolecarbaldehyde	en
dc.subject	DABCO	en
dc.subject	DMAP	en
dc.title	Facile Baylis-Hillman reaction of substituted 3-isoxazolecarbaldehydes: The impact of proximal heteroatom within a heterocycle on the acceleration of reaction	en
dc.type	Article	en