Synthesis of α,β-diamino acid derivatives via asymmetric Mannich reactions of glycine imino esters catalyzed by a chiral phosphoramidite·silver complex


Autoria(s): Cayuelas Rubio, Alberto; Serrano, Loane; Nájera Domingo, Carmen; Sansano, Jose M.
Contribuinte(s)

Universidad de Alicante. Departamento de Química Orgánica

Universidad de Alicante. Instituto Universitario de Síntesis Orgánica

Síntesis Asimétrica (SINTAS)

Data(s)

09/12/2014

09/12/2014

31/12/2014

Resumo

AgOTf·phosphoramidite complexes efficiently catalyze the enantioselective Mannich-type reaction between benzophenone-imine glycine methyl ester and N-tosyl aldimines in the absence of a base. The corresponding syn-adducts, which are the direct precursors of α,β-diamino acids, are obtained with moderate to good syn-diastereoselectivities (up to 9:1) and high enantioselectivities (up to 99% ee).

This work has been supported by the Spanish Ministerio de Ciencia e Innovación (MICINN) (Consolider INGENIO 2010 CSD2007-00006, CTQ2010-20387, CTQ2013-43446-P), FEDER, Generalitat Valenciana (PROMETEO/2009/039, and PROMETEOII 2014/017), and by the University of Alicante. L. S. thanks University of Edinburgh for an ERASMUS fellowship.

Identificador

Tetrahedron: Asymmetry. 2014, 25(24): 1647-1653. doi:10.1016/j.tetasy.2014.11.009

0957-4166 (Print)

1362-511X (Online)

http://hdl.handle.net/10045/43221

10.1016/j.tetasy.2014.11.009

Idioma(s)

eng

Publicador

Elsevier

Relação

http://dx.doi.org/10.1016/j.tetasy.2014.11.009

Direitos

info:eu-repo/semantics/openAccess

Palavras-Chave #Silver #Acid derivatives #Química Orgánica
Tipo

info:eu-repo/semantics/article