A short approach to trisubstituted gamma-butyrolactones

dc.creatorDias, LC
dc.creatorde Castro, IBD
dc.creatorSteil, LJ
dc.creatorAugusto, T
dc.date2006
dc.date39814
dc.date2014-11-17T06:44:41Z
dc.date2015-11-26T16:40:00Z
dc.date2014-11-17T06:44:41Z
dc.date2015-11-26T16:40:00Z
dc.date.accessioned2018-03-28T23:23:47Z
dc.date.available2018-03-28T23:23:47Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 47, n. 2, n. 213, n. 216, 2006.
dc.identifier0040-4039
dc.identifierWOS:000234093100018
dc.identifier10.1016/j.tetlet.2005.10.151
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/53748
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/53748
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/53748
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1272634
dc.descriptionThe dihydroxylation of unsaturated aldol adducts with catalytic OsO4 and NMO occurs under very mild conditions and with moderate to excellent levels of diastereoselectivity to give trisubstituted gamma-butyrolactone derivatives. (c) 2005 Elsevier Ltd. All rights reserved.
dc.description47
dc.description2
dc.description213
dc.description216
dc.languageen
dc.publisherPergamon-elsevier Science Ltd
dc.publisherOxford
dc.publisherInglaterra
dc.relationTetrahedron Letters
dc.relationTetrahedron Lett.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectdihydroxylation
dc.subjectgamma-lactones
dc.subjectosmylation reaction
dc.subjectaldol adducts
dc.subjectEnantioselective Aldol Condensations
dc.subjectL-tartaric Acid
dc.subjectAsymmetric-synthesis
dc.subjectNatural-products
dc.subjectOrganic-synthesis
dc.subjectFacile Synthesis
dc.subjectLactones
dc.subjectStrategy
dc.subject(+)-blastmycinone
dc.subjectLactonization
dc.titleA short approach to trisubstituted gamma-butyrolactones
dc.typeArtículos de revistas


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