Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes

Show simple item record

dc.contributor.author Ali, Bakhat
dc.contributor.author Zukerman-Schpector, Julio
dc.contributor.author Ferreira, Fernando P. [UNIFESP]
dc.contributor.author Shamim, Anwar
dc.contributor.author Pimenta, Daniel C.
dc.contributor.author Stefani, Helici A.
dc.date.accessioned 2016-01-24T14:40:05Z
dc.date.available 2016-01-24T14:40:05Z
dc.date.issued 2015-02-25
dc.identifier http://dx.doi.org/10.1016/j.tetlet.2015.01.059
dc.identifier.citation Tetrahedron Letters. Oxford: Pergamon-Elsevier B.V., v. 56, n. 9, p. 1153-1158, 2015.
dc.identifier.issn 0040-4039
dc.identifier.uri http://repositorio.unifesp.br/handle/11600/38774
dc.description.abstract The cyclodimerization reaction of N-substituted-5-hydroxy-pyrrolydinones promoted by BF3 center dot Et2O and HCl to obtain symmetrical 1,4-dioxane derivatives was achieved in moderate to good yields, mild conditions, and short reaction times. These transformations render a promising alternative route that provides access to diverse 1,4-dioxane derivatives with a wide structural diversity. (C) 2015 Elsevier B.V. All rights reserved. en
dc.description.sponsorship Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorship Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorship FINEP
dc.format.extent 1153-1158
dc.language.iso eng
dc.publisher Elsevier B.V.
dc.relation.ispartof Tetrahedron Letters
dc.rights Acesso restrito
dc.subject Amines en
dc.subject N-Acyliminium en
dc.subject Acid catalysis en
dc.subject Cyclodimerization en
dc.subject 1,4-Dioxane en
dc.title Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes en
dc.type Artigo
dc.rights.license http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.contributor.institution Universidade de São Paulo (USP)
dc.contributor.institution Universidade Federal de São Carlos (UFSCar)
dc.contributor.institution Universidade Federal de São Paulo (UNIFESP)
dc.contributor.institution Inst Butantan
dc.description.affiliation Univ São Paulo, Fac Ciencias Farmaceut, Dept Farm, São Paulo, SP, Brazil
dc.description.affiliation Univ Fed Sao Carlos, Dept Quim, BR-13560 Sao Carlos, SP, Brazil
dc.description.affiliation Universidade Federal de São Paulo, Dept Biofis, São Paulo, SP, Brazil
dc.description.affiliation Univ São Paulo, Inst Quim, São Paulo, SP, Brazil
dc.description.affiliation Inst Butantan, São Paulo, SP, Brazil
dc.description.affiliationUnifesp Universidade Federal de São Paulo, Dept Biofis, São Paulo, SP, Brazil
dc.description.sponsorshipID FAPESP: 2012/00424-2
dc.description.sponsorshipID FAPESP: 2011/11499-0
dc.description.sponsorshipID FAPESP: -2012/17954-4
dc.description.sponsorshipID CNPq: 308.320/2010-7
dc.description.sponsorshipID CNPq: 305626/2013-2
dc.description.sponsorshipID FINEP: 01.09.0278.04
dc.identifier.doi 10.1016/j.tetlet.2015.01.059
dc.description.source Web of Science
dc.identifier.wos WOS:000350087800027



File

File Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record

Search


Browse

Statistics

My Account