THE TAUTOMERISM OF HYDROXY DERIVATIVES OF FIVE-MEMBERED OXYGEN, NIRTOGEN, AND SULFUR HETEROCYCLES

DOI: 10.1016/S0040-4039(00)84773-5

Source and publish data:

Tetrahedron Letters p. 3275 - 3278 (1986)

Update date:2022-08-04

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Authors:

Capon, Brian

Kwok, Fu-Chiu

Road, Pokfulam

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Article abstract of DOI:10.1016/S0040-4039(00)84773-5

The unstable enolic tautomers 3-hydroxyfuran, 2- and 3-hydroxy-thiophene, 3-hydroxy-pyrrole, 3-hydroxy-1-methyl-pyrrole and their benzo-derivatives have been generated in solution and the rate and equilibrium constants for their ketoization determined.

Full text of DOI:10.1016/S0040-4039(00)84773-5

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