Stereoselective transformation of Baylis-Hillman adducts into (3E)-3- (alkoxymethyl)alk-3-en-2-ones

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Suguna Hyma, Rachakonda
dc.contributor.author Muthukumaran, Kannan
dc.contributor.author Kumaragurubaran, Nagaswamy
dc.date.accessioned 2022-03-27T09:03:38Z
dc.date.available 2022-03-27T09:03:38Z
dc.date.issued 2000-01-01
dc.description.abstract The pure (3E)-3-(methoxymethyl)alk-3-en-2-ones and (3E)-3- (ethoxymethyl)alk-3-en-2-ones are formed in the acid induced reaction of 4- hydroxy-3-methylenealkan-2-ones with methanol and ethanol, respectively.
dc.identifier.citation Synthesis
dc.identifier.issn 00397881
dc.identifier.uri 10.1055/s-2000-6248
dc.identifier.uri http://www.thieme-connect.de/DOI/DOI?10.1055/s-2000-6248
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12349
dc.subject (3E)-3-(alkoxymethyl)alk-3-en- 2-ones
dc.subject Alcoholysis
dc.subject Baylis-Hillman reaction
dc.subject Stereoselectivity
dc.subject Trisubstituted alkenes
dc.title Stereoselective transformation of Baylis-Hillman adducts into (3E)-3- (alkoxymethyl)alk-3-en-2-ones
dc.type Journal. Article
dspace.entity.type
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