Nucleophilic addition of triethyl phosphite to acetates of the Baylis-Hillman adducts: Stereoselective synthesis of (E)- and (Z)-allylphosphonates

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Pandiaraju, Subramanian
dc.date.accessioned 2022-03-27T09:04:02Z
dc.date.available 2022-03-27T09:04:02Z
dc.date.issued 1996-02-05
dc.description.abstract Nucleophilic addition of triethyl phosphite to 3-acetoxy-2-methylenealkanenitriles and methyl 3-acetoxy-2-methylenealkanoates provides (2E)-2-(diethoxyphosphorylmethyl)alk-2-enenitriles and methyl (2Z)-2-(diethoxyphosphorylmethyl)alk-2-enoates respectively with good stereoselectivity.
dc.identifier.citation Tetrahedron. v.52(6)
dc.identifier.issn 00404020
dc.identifier.uri 10.1016/0040-4020(95)01055-6
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/0040402095010556
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12360
dc.title Nucleophilic addition of triethyl phosphite to acetates of the Baylis-Hillman adducts: Stereoselective synthesis of (E)- and (Z)-allylphosphonates
dc.type Journal. Article
dspace.entity.type
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