Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/3864
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dc.contributor.authorC., Nativien_us
dc.contributor.authorG., Palioen_us
dc.contributor.authorTaddei, Maurizioen_us
dc.date.accessioned2021-03-30T14:36:09Z-
dc.date.available2021-03-30T14:36:09Z-
dc.date.issued1991-
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/3864-
dc.description45938en_US
dc.description.abstractThe presence of a stereocenter close to the double bond of an allylsilane has an influence on the stereochemistry of the reaction with electrophiles. The stereoselectivity follows the rule of electrophilic attack on a trigonal carbon adjacent to a stereogenic center proposed by Houk. From chiral allylsilanes and achiral aldehydes it is possible to prepare homo allyl alcohols with three stereocenters with a good stereoselectivity.en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofTETRAHEDRON LETTERSen_US
dc.titleAcyclic Stereoselection In the Reaction of Chiral Allylsilanes With Electrophilesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0040-4039(00)74278-Xen_US
dc.identifier.scopus2-s2.0-0026065102en_US
dc.identifier.isiWOS:A1991FD47600015en_US
dc.relation.volume32en_US
dc.description.firstpage1583en_US
dc.description.lastpage1586en_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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