dc.creator | Correia, CRD | |
dc.creator | Oliveira, CC | |
dc.creator | Salles, AG | |
dc.creator | Santos, EAF | |
dc.date | 2012 | |
dc.date | 46539 | |
dc.date | 2014-07-30T19:41:15Z | |
dc.date | 2015-11-26T16:55:34Z | |
dc.date | 2014-07-30T19:41:15Z | |
dc.date | 2015-11-26T16:55:34Z | |
dc.date.accessioned | 2018-03-28T23:43:00Z | |
dc.date.available | 2018-03-28T23:43:00Z | |
dc.identifier | Tetrahedron Letters. Pergamon-elsevier Science Ltd, v. 53, n. 26, n. 3325, n. 3328, 2012. | |
dc.identifier | 0040-4039 | |
dc.identifier | WOS:000304851500031 | |
dc.identifier | 10.1016/j.tetlet.2012.04.079 | |
dc.identifier | http://www.repositorio.unicamp.br/jspui/handle/REPOSIP/73651 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/73651 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1277160 | |
dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description | Successful enantioselective Heck-Matsuda arylations were accomplished for the first time using chiral bisoxazolines as ligands. Enantioselective Heck arylations were performed with several cyclic nonactivated olefins to provide the Heck products in 63-96% isolated yields and in enantiomeric excesses of 54% up to 84%. (C) 2012 Elsevier Ltd. All rights reserved. | |
dc.description | 53 | |
dc.description | 26 | |
dc.description | 3325 | |
dc.description | 3328 | |
dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.language | en | |
dc.publisher | Pergamon-elsevier Science Ltd | |
dc.publisher | Oxford | |
dc.publisher | Inglaterra | |
dc.relation | Tetrahedron Letters | |
dc.relation | Tetrahedron Lett. | |
dc.rights | fechado | |
dc.rights | http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy | |
dc.source | Web of Science | |
dc.subject | Enantioselective Heck-Matsuda | |
dc.subject | Bisoxazolines | |
dc.subject | Arenediazonium salts | |
dc.subject | Catalytic Asymmetric-synthesis | |
dc.subject | Bis(oxazoline) Copper(ii) Complexes | |
dc.subject | Diazonium Salts | |
dc.subject | Decalin Derivatives | |
dc.subject | Palladium | |
dc.subject | Michael | |
dc.subject | Analogs | |
dc.subject | Ligand | |
dc.subject | Ester | |
dc.subject | Ions | |
dc.title | The first examples of the enantioselective Heck-Matsuda reaction: arylation of unactivated cyclic olefins using chiral bisoxazolines | |
dc.type | Artículos de revistas | |