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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Multicomponent Combinatorial Development and Conformational Analysis of Prolyl Peptide-Peptoid Hybrid Catalysts: Application in the Direct Asymmetric Michael Addition

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Autor(es):
de la Torre, Alexander F. [1] ; Rivera, Daniel G. [1, 2] ; Ferreira, Marco A. B. [1] ; Correa, Arlene G. [1] ; Paixao, Marcio W. [1]
Número total de Autores: 5
Afiliação do(s) autor(es):
[1] Univ Fed Sao Carlos, Dept Quim, BR-13565905 Sao Carlos, SP - Brazil
[2] Univ Havana, Fac Chem, Ctr Nat Prod Study, Havana 10400 - Cuba
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: Journal of Organic Chemistry; v. 78, n. 20, p. 10221-10232, OCT 18 2013.
Citações Web of Science: 19
Resumo

A solution-phase combinatorial approach based on the Ugi four-component reaction was implemented for the development of new prolyl peptide-peptoid hybrid catalysts. Three different elements of diversity were varied during the creation of the set of catalysts: the amine, oxo, and isocyano components. The multicomponent nature of this process enabled the straightforward generation of a series of peptide-peptoid hybrids having the generic sequence Pro-N-R-1-Xaa-NHR3, with Xaa being either Gly (R-2 = H) or Aib (R-2 = gem-Me) and R-1 and R-3 either alkyl or amino acid substituents. The catalytic behavior of the peptide-peptoid hybrids was assessed in the asymmetric conjugate addition of aldehydes to nitroolefins, where most of the catalysts showed great efficacy and rendered the Michael adducts with good to excellent enantio- and diastereoselectivity. A molecular modeling study was performed for two distinct catalysts aiming to understand their conformational features. The conformational analysis provided important information for understanding the remarkable stereocontrol achieved during the organocatalytic transformation. (AU)

Processo FAPESP: 09/07281-0 - Organocatálise assimétrica: preparação de novos organocatalisadores e desenvolvimento de novas metodologias
Beneficiário:Márcio Weber Paixão
Linha de fomento: Auxílio à Pesquisa - Apoio a Jovens Pesquisadores
Processo FAPESP: 13/02311-3 - Novas abordagens na síntese assimétrica de tetraidrofuranos e tetraidropiranos substituídos com potencial aplicação na preparação de moléculas bioativas
Beneficiário:Marco Antonio Barbosa Ferreira
Linha de fomento: Auxílio à Pesquisa - Regular