Literature DB >> 23033139

Organocatalyzed enantioselective desymmetrization of diols in the preparation of chiral building blocks.

María D Díaz-de-Villegas1, José A Gálvez, Ramón Badorrey, M Pilar López-Ram-de-Víu.   

Abstract

Desymmetrization of diols is a powerful tool to the synthesis of chiral building blocks. Among the different approaches to perform discrimination between both enantiotopic hydroxyl groups, the organocatalytic approach has gained importance in the last years. A diverse range of organocatalysts has been used to efficiently promote this enantioselective transformation and this Minireview examines the different contributions in this field.
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Year:  2012        PMID: 23033139     DOI: 10.1002/chem.201202264

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


  5 in total

1.  Resolution of terminal 1,2-diols via silyl transfer.

Authors:  Xixi Sun; Amanda D Worthy; Kian L Tan
Journal:  J Org Chem       Date:  2013-10-02       Impact factor: 4.354

2.  Alkylative kinetic resolution of vicinal diols under phase-transfer conditions: a chiral ammonium borinate catalysis.

Authors:  Martin Pawliczek; Takuya Hashimoto; Keiji Maruoka
Journal:  Chem Sci       Date:  2017-12-12       Impact factor: 9.825

3.  Catalytic Asymmetric β-Oxygen Elimination.

Authors:  Christof Matt; Andreas Orthaber; Jan Streuff
Journal:  Angew Chem Int Ed Engl       Date:  2022-03-25       Impact factor: 16.823

Review 4.  Organocatalyzed enantioselective desymmetrization of aziridines and epoxides.

Authors:  Ping-An Wang
Journal:  Beilstein J Org Chem       Date:  2013-08-15       Impact factor: 2.883

5.  Enantioselective silyl protection of alcohols promoted by a combination of chiral and achiral Lewis basic catalysts.

Authors:  Nathan Manville; Hekla Alite; Fredrik Haeffner; Amir H Hoveyda; Marc L Snapper
Journal:  Nat Chem       Date:  2013-07-28       Impact factor: 24.427

  5 in total

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