Determination of the Absolute Configuration of beta-Chiral Primary Alcohols Using the Competing Enantioselective Conversion Method

摘要

A method for determining the absolute configuration of beta-chiral primary alcohols has been developed. Enantioenriched alcohols were acylated in the presence of either enantiomer of the enantioselective acylation catalyst HBTM, and the faster reaction was determined by measuring product conversion using 1H NMR spectroscopic analysis. An empirical mnemonic was developed that correlates the absolute configuration of the alcohol to the faster reacting catalyst. Successful substrates for this method include primary alcohols that bear a directing group on the stereogenic center; directing groups include arenes, heteroarenes, enones, and halides.