Aldol Reactions of Conformationally Stable Axially Chiral Thiohydantoin Derivatives.

ABSTRACT: Two novel axially chiral ortho-trifluoromethylphenyl thiohydantoin derivatives have been prepared atroposelectively from the reaction of R and S alanine methyl ester HCl salts with ortho-trifluoromethylphenyl isothiocyanate in the presence of triethyl amine. It was found that after purification of the crude product by simple recrystallization, the R amino acid esters yielded thiohydantoins having solely M axial chirality whereas the S ones returned the P isomers only. This result prompted us to perform sterically controlled aldol reactions on M and P thiohydantoin atropisomers. It was found that during the aldol reaction of 3-o-trifluoromethyl-5-methylthiohydantoins, the o-trifluoromethyl group of the M<

SUBMITTER: Sarigul Ozbek S 

PROVIDER: S-EPMC8552363 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature