The Baylis-Hillman chemistry in aqueous media: A convenient synthesis of 2-methylenealkanoates and alkanenitriles

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Kumaragurubaran, Nagaswamy
dc.date.accessioned 2022-03-27T09:03:16Z
dc.date.available 2022-03-27T09:03:16Z
dc.date.issued 2001-01-15
dc.description.abstract A convenient, general and efficient synthesis of 2-methylenealkanoates and alkanenitriles is accomplished via the regioselective nucleophilic (SN2′) addition of hydride ion from NaBH4 to (2Z)-2-(bromomethyl)alk-2-enoates and 2-(bromomethyl)alk-2-enenitriles respectively in the presence of DABCO in environment friendly aqueous media. Synthesis of two hypoglycemic agents is also described. © 2001 Elsevier Science Ltd.
dc.identifier.citation Tetrahedron Letters. v.42(3)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/S0040-4039(00)01967-5
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403900019675
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12338
dc.subject 2-Methylenealkanoates
dc.subject Alkanenitriles
dc.subject Baylis-Hillman chemistry
dc.subject Regioselectivity
dc.title The Baylis-Hillman chemistry in aqueous media: A convenient synthesis of 2-methylenealkanoates and alkanenitriles
dc.type Journal. Article
dspace.entity.type
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