A rapid and high-yielding synthesis of β-hydroxyselenides by regio- and stereoselective ring-opening of epoxides with benzeneselenol using ammonium-12-molybdophosphate

β-Hydroxyselenides have conveniently been synthesized within a short period of time and in excellent yields by regio- and stereoselective ring-opening of epoxides with benzeneselenol at room temperature in the presence of ammonium-12-molybdophosphate (AMP) as a heterogeneous catalyst.

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Bibliographic Details
Published in:Journal of molecular catalysis. A, Chemical Chemical, 2007-02, Vol.263 (1), p.276-278
Main Authors: Das, Biswanath, Reddy, V. Saidi, Ramu, R.
Format: Article
Language:English
Subjects:
Ammonium-12-molybdophosphate
Benzeneselenol
Catalysis
Chemistry
Epoxide
Exact sciences and technology
General and physical chemistry
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
β-Hydroxyselenide
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Description
Summary:β-Hydroxyselenides have conveniently been synthesized within a short period of time and in excellent yields by regio- and stereoselective ring-opening of epoxides with benzeneselenol at room temperature in the presence of ammonium-12-molybdophosphate (AMP) as a heterogeneous catalyst.
ISSN:1381-1169
1873-314X
DOI:10.1016/j.molcata.2006.08.091