B. Klotzberendes et al., ENZYMATIC-SYNTHESIS OF OPTICALLY-ACTIVE MONO-ALKYLATED MALONIC MONOESTERS, Tetrahedron : asymmetry, 8(11), 1997, pp. 1821-1823
Pig-liver esterase hydrolysis of tertiary-alkyl malonic diesters 1 lea
ds to malonic monoesters 2 in high yields and with enantiomeric excess
es up to 96% ee. The configuration of the new stereogenic carbon atom
was determined by crystal structure analysis of the (S)-1-phenylethyla
mide of 2b. The monoesters 2 are stable against racemisation between p
H 2 to pH 12 as shown for 2b. (C) 1997 Elsevier Science Ltd.