Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/119967
Full metadata record
DC FieldValueLanguage
dc.contributor.authorValero González, Guillem-
dc.contributor.authorLeón, Carlos M.-
dc.contributor.authorMoyano i Baldoire, Albert-
dc.date.accessioned2018-02-19T11:19:17Z-
dc.date.available2018-02-19T11:19:17Z-
dc.date.issued2015-06-12-
dc.identifier.issn2300-4630-
dc.identifier.urihttp://hdl.handle.net/2445/119967-
dc.description.abstractSolvent effects in the L-tryptophan-catalyzed Mannich reaction between hydroxyacetone and glyoxylate imines have been examined. The use of a DMSO/1-butanol (4:1 v/v) mixture as solvent at rt provided the expected Mannich adducts in good yields, high anti-diastereoselectivity (up to 10.3:1 anti/syn ratio) and excellent enantioselectivities (up to >99.9% ee for the anti isomer)-
dc.format.extent10 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherDe Gruyter Open-
dc.relation.isformatofhttps://doi.org/10.1515/asorg-2015-0001-
dc.relation.ispartofAsymmetric Catalysis, 2015, vol. 2, num. 1, p. 7-16-
dc.relation.urihttps://doi.org/10.1515/asorg-2015-0001-
dc.rightscc by-nc-nd (c) Valero González, Guillem et al., 2015-
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/-
dc.sourceArticles publicats en revistes (Química Inorgànica i Orgànica)-
dc.subject.classificationAminoàcids-
dc.subject.classificationCatàlisi asimètrica-
dc.subject.otherAmino acids-
dc.subject.otherEnantioselective catalysis-
dc.titleSolvent-controlled diastereoselectivity in tryptophan-catalyzed Mannich reactions-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec668850-
dc.date.updated2018-02-19T11:19:17Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

Files in This Item:
File Description SizeFormat 
668850.pdf525.43 kBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons