102779-60-2Relevant academic research and scientific papers
STEREOSELECTIVE CONDENSATION OF BIS-p-TOLYLTHIOMETHANE WITH LACTIC ACID DERIVATIVES THROUGH AN ACYLATION-REDUCTION STRATEGY: SYNTHESIS OF PROTECTED 4-DEOXY-L-THREOSE AND 4-DEOXY-L-ERYTHROSE
Guanti, Giuseppe,Banfi, Luca,Guaragna, Alberto,Narisano, Enrica
, p. 2369 - 2376 (2007/10/02)
The condensation of lithium bis-p-tolylthiomethanide with protected ethyl-L-lactates gave a series of 3-alkoxy- (or 3-hydroxy-) 1,1-bis-p-tolylthiobutan-2-ones, which were stereoselectively reduced to the corresponding syn- or anti-alcohols with diastereo
