Literature DB >> 22707074

Chiral quaternary phosphonium salts: a new class of organocatalysts.

Dieter Enders1, Thanh Vinh Nguyen.   

Abstract

Phase-transfer catalysis has widely been used as a prime synthetic tool for both laboratory and industrial processes. During the last twenty years, asymmetric phase-transfer catalysis using chiral organocatalysts has attracted widespread interest. However, the scope of chiral phase-transfer catalysis has been limited mostly to the quaternary ammonium salts. As an emerging area, the recent developments in the application of quaternary phosphonium salts as chiral phase-transfer catalysts are discussed in this article.

Entities:  

Year:  2012        PMID: 22707074     DOI: 10.1039/c2ob25823d

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


  5 in total

Review 1.  Phosphine Organocatalysis.

Authors:  Hongchao Guo; Yi Chiao Fan; Zhanhu Sun; Yang Wu; Ohyun Kwon
Journal:  Chem Rev       Date:  2018-09-27       Impact factor: 60.622

2.  Asymmetric cyclopropanation of chalcones using chiral phase-transfer catalysts.

Authors:  Richard Herchl; Mario Waser
Journal:  Tetrahedron Lett       Date:  2013-05-15       Impact factor: 2.415

3.  Direct 1,1-Bisphosphonation of Isocyanides: Atom- and Step-Economical Access to Bisphosphinoylaminomethanes.

Authors:  Qing Yuan; Hua-Wei Liu; Zhong-Jian Cai; Shun-Jun Ji
Journal:  ACS Omega       Date:  2021-03-17

Review 4.  Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles.

Authors:  Johannes Schörgenhumer; Maximilian Tiffner; Mario Waser
Journal:  Beilstein J Org Chem       Date:  2017-08-22       Impact factor: 2.883

5.  Versatile Visible-Light-Driven Synthesis of Asymmetrical Phosphines and Phosphonium Salts.

Authors:  Percia Beatrice Arockiam; Ulrich Lennert; Christina Graf; Robin Rothfelder; Daniel J Scott; Tillmann G Fischer; Kirsten Zeitler; Robert Wolf
Journal:  Chemistry       Date:  2020-10-30       Impact factor: 5.236

  5 in total

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