Applications of Baylis-Hillman coupling products: A remarkable reversal of stereochemistry from esters to nitriles: A simple synthesis of (2E)-2-methylalk-2-en-1-ols and (2Z)-2-methylalk-2-enenitriles

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Sarma, Pakala K.S.
dc.date.accessioned 2022-03-27T09:04:58Z
dc.date.available 2022-03-27T09:04:58Z
dc.date.issued 1992-12-01
dc.description.abstract Reaction of methyl 3-acetoxy-2-methylenealkanoates with the reducing agent, lithium aluminium hydride (LAH): ethanol (1 : 1), provides (2E)-2-methylalk-2- en-1-ols, whereas, reaction of 3-acetoxy-2-methylenealkanenitriles with the same reagent provides (2Z)-2-methylalk-2-enenitriles in high yields.
dc.identifier.citation Journal of the Chemical Society, Chemical Communications
dc.identifier.issn 00224936
dc.identifier.uri 10.1039/C39920000955
dc.identifier.uri http://xlink.rsc.org/?DOI=C39920000955
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12384
dc.title Applications of Baylis-Hillman coupling products: A remarkable reversal of stereochemistry from esters to nitriles: A simple synthesis of (2E)-2-methylalk-2-en-1-ols and (2Z)-2-methylalk-2-enenitriles
dc.type Journal. Article
dspace.entity.type
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