Synthesis of α,β-diamino acid derivatives via asymmetric Mannich reactions of glycine imino esters catalyzed by a chiral phosphoramidite·silver complex
Contribuinte(s) |
Universidad de Alicante. Departamento de Química Orgánica Universidad de Alicante. Instituto Universitario de Síntesis Orgánica Síntesis Asimétrica (SINTAS) |
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Data(s) |
09/12/2014
09/12/2014
31/12/2014
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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 |