Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4014
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dc.contributor.authorF., Danielloen_us
dc.contributor.authorA., Mannen_us
dc.contributor.authorTaddei, Maurizioen_us
dc.contributor.authorC. G., Wermuthen_us
dc.date.accessioned2021-03-30T14:41:08Z-
dc.date.available2021-03-30T14:41:08Z-
dc.date.issued1994-
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/4014-
dc.description45954en_US
dc.description.abstractBromoallenes 3a and 3b derived from (D)-Serine undergo S(N)2' alkylation with organo copper reagents to give alkynyl amino alcohol derivatives. These compounds can be further transformed into blanched enantiomerically enriched alpha-amino acids as, for example (L)-Isolcucine and (L)-Alloisoleucine.en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofTETRAHEDRON LETTERSen_US
dc.title1,3-diastereocontrol With Bromoallenes - Synthesis of Enantiomerically Pure Beta-branched Alpha-amino-acidsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0040-4039(00)77369-2en_US
dc.identifier.scopus2-s2.0-0027973726en_US
dc.identifier.isiWOS:A1994PM95300019en_US
dc.relation.volume35en_US
dc.description.firstpage7775en_US
dc.description.lastpage7778en_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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