Chemistry of Heterocyclic Compounds p. 775 - 778 (2000)
Update date:2022-08-11
Topics:
Lebedev
Leite
Fleisher
Stonkus
The relative stability of 2-hydroxytetrahydrofuran and the tautomeric 4-hydroxybutanal was determined by the semi-empirical AM1 method. It was concluded that the cyclic tautomer predominates in the gas phase at 25°C. Vapor-phase dehydration of 2-hydroxytetrahydrofuran in the presence of porcelain and silica gel L leads to a quantitative yield of 2,3-dihydrofuran.
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Doi:10.1166/jnn.2019.16688
(2019)Doi:10.1055/s-2001-18062
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(2020)Doi:10.1016/S0040-4039(00)97755-4
(1990)Doi:10.1002/mrc.1260260515
(1988)
