Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4166
DC FieldValueLanguage
dc.contributor.authorA., Mannen_us
dc.contributor.authorL., Quarantaen_us
dc.contributor.authorG., Reginatoen_us
dc.contributor.authorTaddei, Maurizioen_us
dc.date.accessioned2021-03-30T14:42:10Z-
dc.date.available2021-03-30T14:42:10Z-
dc.date.issued1996-
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/4166-
dc.description45959en_US
dc.description.abstractMolecules structurally analogous to dipeptides, containing an oxirane ring in the place of the peptidic bond, can be prepared by oxidative conversion of beta-hydroxyselenides obtained by Mukaiyama aldol type reaction of N-protected beta-amino alpha-selenyl aldehydes derived from naturally occurring amino acids. Copyright (C) 1996 Elsevier Science Ltden_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofTETRAHEDRON LETTERSen_US
dc.titleA general synthesis of oligopeptides containing an oxirane ring in the place of a peptidic bonden_US
dc.typeArticleen_US
dc.identifier.doi10.1016/0040-4039(96)00352-8en_US
dc.identifier.scopus2-s2.0-0029991378en_US
dc.identifier.isiWOS:A1996UE23300039en_US
dc.relation.volume37en_US
dc.description.firstpage2651en_US
dc.description.lastpage2654en_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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