Baylis-Hillman chemistry: A novel synthesis of functionalized 1,4-pentadienes

dc.contributor.author	Basavaiah, Deevi
dc.contributor.author	Kumaragurubaran, Nagaswamy
dc.contributor.author	Sharada, Duddu S.
dc.date.accessioned	2022-03-27T09:03:20Z
dc.date.available	2022-03-27T09:03:20Z
dc.date.issued	2001-01-01
dc.description.abstract	A novel synthesis of functionalized 1,4-pentadienes via the reaction of acrylonitrile with allyl halides, derived from Baylis-Hillman adducts, in the presence of DABCO has been described, demonstrating for the first time the application of allyl halides as electrophiles in the Baylis-Hillman reaction. © 2000 Elsevier Science Ltd.
dc.identifier.citation	Tetrahedron Letters. v.42(1)
dc.identifier.issn	00404039
dc.identifier.uri	10.1016/S0040-4039(00)01886-4
dc.identifier.uri	https://www.sciencedirect.com/science/article/abs/pii/S0040403900018864
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/12340
dc.subject	Acrylonitrile
dc.subject	Baylis-Hillman chemistry
dc.subject	DABCO
dc.subject	Functionalized 1,4-pentadienes
dc.title	Baylis-Hillman chemistry: A novel synthesis of functionalized 1,4-pentadienes
dc.type	Journal. Article
dspace.entity.type

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