Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/3968
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dc.contributor.authorF., Danielloen_us
dc.contributor.authorD., Mattiien_us
dc.contributor.authorTaddei, Maurizioen_us
dc.date.accessioned2021-03-30T14:36:35Z-
dc.date.available2021-03-30T14:36:35Z-
dc.date.issued1993-
dc.identifier.issn0936-5214en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/3968-
dc.description45944en_US
dc.description.abstractThe title reagent was used in reaction with aldehydes in the presence of BF3. OEt2 to give hydroxy allylic chlorides which were further transformed into tetrahydrofurans using DBU and LiClO4. Alternatively butyrolactones could be prepared from the same intermediates after oxidation of the chloro allylic functionality. Starting from isoleucine we prepared a methylenebutyrolactone which has been used in the synthesis of several enzyme inhibitors.en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofSYNLETTen_US
dc.title2-(chloromethyl)-2-(trimethylsilyl)-1-propene - A Convenient Reagent For the Synthesis of Methylenetetrahydrofurans and Methylenebutyrolactonesen_US
dc.typeArticleen_US
dc.identifier.scopus2-s2.0-0001556010en_US
dc.identifier.isiWOS:A1993KM50400009en_US
dc.description.firstpage119en_US
dc.description.lastpage121en_US
dc.description.thirdmissionNot applicableen_US
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.fulltextNo Fulltext-
crisitem.author.orcid0000-0001-8660-7580-
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