Literature DB >> 24089249

Catalytic enantioselective reductive desymmetrisation of achiral and meso compounds.

Héctor Fernández-Pérez1, Pablo Etayo, Joan R Lao, José L Núñez-Rico, Anton Vidal-Ferran.   

Abstract

Herein an overview of reductive catalytic enantioselective desymmetrisation of achiral or meso compounds is provided. The most efficient reductive desymmetrisations described in the literature, which involve the reduction of C=O, C=N, C=C and C-halogen bonds, or reductive ring-opening, are summarised. The structural diversity of the valuable highly enantioenriched intermediates prepared by reductive desymmetrisation is highlighted.

Entities:  

Year:  2013        PMID: 24089249     DOI: 10.1039/c3cc45466e

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Enantioselective desymmetrization via carbonyl-directed catalytic asymmetric hydroboration and Suzuki-Miyaura cross-coupling.

Authors:  Gia L Hoang; Zhao-Di Yang; Sean M Smith; Rhitankar Pal; Judy L Miska; Damaris E Pérez; Libbie S W Pelter; Xiao Cheng Zeng; James M Takacs
Journal:  Org Lett       Date:  2015-02-02       Impact factor: 6.005

2.  Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis.

Authors:  Jiajie Feng; Michael Holmes; Michael J Krische
Journal:  Chem Rev       Date:  2017-09-14       Impact factor: 60.622

3.  Differentiation of Epoxide Enantiomers in the Confined Spaces of an Homochiral Cu(II) Metal-Organic Framework by Kinetic Resolution.

Authors:  Juanjo Cabezas-Giménez; Vanesa Lillo; José Luis Núñez-Rico; M Nieves Corella-Ochoa; Jesús Jover; José Ramón Galán-Mascarós; Anton Vidal-Ferran
Journal:  Chemistry       Date:  2021-07-09       Impact factor: 5.020

  3 in total

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