Epoxidation of 2-aryl-4-methyl-3,6-dihydropyrans and reaction of the products with piperidine

Authors :: M. G. Safarov
S. A. Vasil'eva
T. B. Semenov
L. V. Syurina
U. G. Ubatullin
Source :: Chemistry of Heterocyclic Compounds. 20:1200-1202
Publication Year :: 1984
Publisher :: Springer Science and Business Media LLC, 1984.
Abstract: 2-Aryl-4-methyl-4,5-epoxytetrahydropyrans, which react with piperidine regioselectively with trans-diaxial cleavage of the oxide ring at the least substituted carbon atom, were synthesized by the reaction of 2-aryl-4-methyl-3,6-dihydropyrans with peracids.

Subjects :: chemistry.chemical_compound
Carbon atom
chemistry
Aryl
Organic Chemistry
Oxide
Piperidine
Ring (chemistry)
Cleavage (embryo)
Medicinal chemistry

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