Literature DB >> 31449414

Axially Chiral Trifluoromethylbenzimidazolylbenzoic Acid: A Chiral Derivatizing Agent for α-Chiral Primary Amines and Secondary Alcohols To Determine the Absolute Configuration.

Michal Kriegelstein1, David Profous1, Antonín Lyčka2, Zdeněk Trávníček3, Adam Přibylka1, Tereza Volná4, Sandra Benická4, Petr Cankař1.   

Abstract

Racemic 2-(2-trifluoromethyl)-1H-benzo[d]imidazol-1-yl)benzoic acid (TBBA) was synthesized in three steps from 1-fluoro-2-nitrobenzene. Target (P)- and (M)-TBBA atropisomers were stable with a racemization barrier above 30 kcal/mol. As a chiral derivatizing agent, TBBA showed much higher differences in chemical shifts (ΔδPM) than the conventional Mosher's acid.

Entities:  

Year:  2019        PMID: 31449414     DOI: 10.1021/acs.joc.9b01770

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Limitations of Trifluoromethylbenzoimidazolylbenzoic Acid as a Chiral Derivatizing Agent to Assign Absolute Configuration for β-Chiral Aminoalcohols.

Authors:  Michal Kriegelstein; David Profous; Adam Přibylka; Antonín Lyčka; Petr Cankař
Journal:  ACS Omega       Date:  2022-04-04
  1 in total

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