A STUDY OF THE TAUTOMERISM OF 2- AND 4-ETHOXYCARBONYLTHIOLAN-3-ONES IMPLICATING STEREOCHEMICAL EFFECTS OF RING-SUBSTITUTION

DOI: 10.1016/S0040-4020(01)98968-9

Source and publish data:

Tetrahedron p. 2633 - 2640 (1981)

Update date:2022-08-02

Topics:: Authors:

DUUS, F.

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Article abstract of DOI:10.1016/S0040-4020(01)98968-9

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-

Full text of DOI:10.1016/S0040-4020(01)98968-9

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A STUDY OF THE TAUTOMERISM OF 2- AND 4-ETHOXYCARBONYLTHIOLAN-3-ONES IMPLICATING STEREOCHEMICAL EFFECTS OF RING-SUBSTITUTION

DOI: 10.1016/S0040-4020(01)98968-9

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4020(01)98968-9

Full text of DOI:10.1016/S0040-4020(01)98968-9

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