Literature DB >> 25411063

Aminocatalysis: beyond steric shielding and hydrogen-bonding.

Bruno Matos Paz1, Hao Jiang, Karl Anker Jørgensen.   

Abstract

The stereochemical outcome of most aminocatalytic transformations is determined by the steric-shielding or hydrogen-directing approach. However, in recent years several reactions have appeared in which the stereochemical outcome is beyond these two approaches. This Concept article will highlight such reactions and postulate that the stereochemical outcome can be accounted for by electrostatic interactions between the catalyst-bound substrate and the reagent in the transition state.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  aminocatalysis; electrostatic interactions; oganocatalysis; stereochemistry

Year:  2014        PMID: 25411063     DOI: 10.1002/chem.201405038

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Racemic hemiacetals as oxygen-centered pronucleophiles triggering cascade 1,4-addition/Michael reaction through dynamic kinetic resolution under iminium catalysis. Development and mechanistic insights.

Authors:  Ane Orue; Uxue Uria; David Roca-López; Ignacio Delso; Efraím Reyes; Luisa Carrillo; Pedro Merino; Jose L Vicario
Journal:  Chem Sci       Date:  2017-01-30       Impact factor: 9.825

2.  Synthesis of new pyrrolidine-based organocatalysts and study of their use in the asymmetric Michael addition of aldehydes to nitroolefins.

Authors:  Alejandro Castán; Ramón Badorrey; José A Gálvez; María D Díaz-de-Villegas
Journal:  Beilstein J Org Chem       Date:  2017-03-27       Impact factor: 2.883

  2 in total

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