You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/116965
Full metadata record
DC FieldValueLanguage
dc.contributor.authorFeltrin, M. P.-
dc.contributor.authorAlmeida, W. P.-
dc.date.accessioned2015-03-18T15:54:34Z-
dc.date.accessioned2016-10-25T20:28:30Z-
dc.date.available2015-03-18T15:54:34Z-
dc.date.available2016-10-25T20:28:30Z-
dc.date.issued2003-01-01-
dc.identifierhttp://dx.doi.org/10.1081/SCC-120017189-
dc.identifier.citationSynthetic Communications. New York: Marcel Dekker Inc, v. 33, n. 7, p. 1141-1146, 2003.-
dc.identifier.issn0039-7911-
dc.identifier.urihttp://hdl.handle.net/11449/116965-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/116965-
dc.description.abstractA synthesis of the antihipertensive amide 1, named captopril, is described. The strategy is based on a Baylis-Hillman reaction between N-acryloylproline and formaldehyde. Subsequential diastereoselective hydrogenation step and functional group interconversion provided captopril in good overall yield.en
dc.format.extent1141-1146-
dc.language.isoeng-
dc.publisherMarcel Dekker Inc-
dc.sourceWeb of Science-
dc.titleA synthesis of captopril through a Baylis-Hillman reactionen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Estadual Paulista, Inst Ciencias Saude, BR-13055044 Campinas, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Inst Ciencias Saude, BR-13055044 Campinas, SP, Brazil-
dc.identifier.doi10.1081/SCC-120017189-
dc.identifier.wosWOS:000182804200011-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofSynthetic Communications-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
Show simple item record Show full item record   View Statistics
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.