80278-79-1Relevant articles and documents
A STUDY OF THE TAUTOMERISM OF 2- AND 4-ETHOXYCARBONYLTHIOLAN-3-ONES IMPLICATING STEREOCHEMICAL EFFECTS OF RING-SUBSTITUTION
DUUS, F.
, p. 2633 - 2640 (1981)
A series of 2- and 4-ethoxycarbonylthiolan-3-ones have been synthesized and studied by 1H NMR and IR spectroscopy.Under conditions of tautomeric equilibrium in tetrachloromethane solution the 4-ethoxycarbonylthiolan-3-ones are generally more enolized (40-