| Literature DB >> 31449414 |
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