NaBH4 reduction of one ketone in 1, 4-diacetylbenzene followed by Amano PS catalyzed acylation of the R enantiomer, separation of the R acetate from the S alcohol, and reduction of the remaining ketone in each with NaBD4 has provided two mixtures of monodeuterated diol diastereomers: R, R (d) plus R, S (d) and S, R (d) plus S, S (d). Conversion of the unseparated diols into their bis-(R)-MTPA (mosher's) esters has allowed the NMR signals ...