Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4375
DC FieldValueLanguage
dc.contributor.authorM., Demarcusen_us
dc.contributor.authorS. N., Filighedduen_us
dc.contributor.authorA., Mannen_us
dc.contributor.authorTaddei, Maurizioen_us
dc.date.accessioned2021-03-30T14:43:36Z-
dc.date.available2021-03-30T14:43:36Z-
dc.date.issued1999-
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/4375-
dc.description45977en_US
dc.description.abstract(E)-Methoxy alkenes derived from N-Boc or NCbz alpha-amino acids undergo stereoselective addition of phenyl selenyl chloride in the presence of Ti(Oi-Pr)(4) and LiCl to give the corresponding phenylselenyl aldehydes that can be easily transformed into new enantiomericalIy pure amino acids containing an aziridine ring. (C) 1999 Elsevier Science Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofTETRAHEDRON LETTERSen_US
dc.titleStereoselective addition of phenyl selenyl chloride to methoxy alkenes derived from N-protected chiral alpha-amino acids.en_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0040-4039(99)00761-3en_US
dc.identifier.scopus2-s2.0-0033522959en_US
dc.identifier.isiWOS:000080436400038en_US
dc.relation.volume40en_US
dc.description.firstpage4417en_US
dc.description.lastpage4420en_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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