Baylis-Hillman chemistry: A convenient stereoselective synthesis of (Z,Z)- and (E,E)-1,4-diallylpiperazines

dc.contributor.author	Basavaiah, D.
dc.contributor.author	Reddy, R. M.
dc.date.accessioned	2022-03-27T09:03:03Z
dc.date.available	2022-03-27T09:03:03Z
dc.date.issued	2001-11-12
dc.description.abstract	Treatment of piperazine with 3-acetoxy-2-methylenealkanenitriles provides exclusively (1,4)-bis[(2Z)-2-cyanoalk-2-en-1-yl]piperazines. A similar reaction of methyl 3-acetoxy-3-aryl-2-methylenepropanoates with piperazine produces (1,4)-bis[(2E)-3-aryl-2-methoxycarbonylprop-2-en-1-yl]piperazines as the major products.
dc.identifier.citation	Journal of Chemical Research - Part S
dc.identifier.issn	03082342
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/12332
dc.subject	Baylis-Hillman chemistry
dc.subject	Bisallylamines
dc.subject	Piperazine
dc.subject	Stereoselectivity
dc.title	Baylis-Hillman chemistry: A convenient stereoselective synthesis of (Z,Z)- and (E,E)-1,4-diallylpiperazines
dc.type	Journal. Article
dspace.entity.type

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