Literature DB >> 22717593

A tripeptide-like prolinamide-thiourea as an aldol reaction catalyst.

Stamatis Fotaras1, Christoforos G Kokotos, George Kokotos.   

Abstract

A tripeptide-like prolinamide-thiourea catalyst with (S)-proline, (1S,2S)-diphenylethylenediamine and (S)-di-tert-butyl aspartate as building blocks provides the products of the reaction between ketones and aromatic aldehydes in high to quantitative yields and high stereoselectivities (up to 99:1 dr and 99% ee). Both the chiral centers of the diamine unit are essential, while the thiourea hydrogen originating from the amine and the amide hydrogen play a predominant role for the catalyst efficiency.

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Year:  2012        PMID: 22717593     DOI: 10.1039/c2ob25693b

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Supported bifunctional thioureas as recoverable and reusable catalysts for enantioselective nitro-Michael reactions.

Authors:  José M Andrés; Miriam Ceballos; Alicia Maestro; Isabel Sanz; Rafael Pedrosa
Journal:  Beilstein J Org Chem       Date:  2016-04-01       Impact factor: 2.883

  1 in total

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