Literature DB >> 12746823

Highly stereoselective tandem aza-Michael addition-enolate protonation to form partially modified retropeptide mimetics incorporating a trifluoroalanine surrogate.

Monica Sani1, Luca Bruché, Gema Chiva, Santos Fustero, Julio Piera, Alessandro Volonterio, Matteo Zanda.   

Abstract

Entities:  

Year:  2003        PMID： 12746823     DOI： 10.1002/anie.200250711

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  2 in total

1.  Integrating the intrinsic conformational preferences of noncoded α-amino acids modified at the peptide bond into the noncoded amino acids database.

Authors:  Guillem Revilla-López; Francisco Rodríguez-Ropero; David Curcó; Juan Torras; M Isabel Calaza; David Zanuy; Ana I Jiménez; Carlos Cativiela; Ruth Nussinov; Carlos Alemán
Journal:  Proteins       Date:  2011-04-12

2.  Efficient synthesis of suitably protected beta-difluoroalanine and gamma-difluorothreonine from L-ascorbic acid.

Authors:  Gongyong Li; Wilfred A van der Donk
Journal:  Org Lett       Date:  2007-01-04       Impact factor: 6.005
  2 in total

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