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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2006 Volume 16, Issue 5, Pages 245–247 (Mi mendc3607)

This article is cited in 6 papers

Solid-state properties of 1,2-epoxy-3-(2-cyanophenoxy)propane, a conglomerate-forming chiral drug precursor

A. A. Bredikhin, Z. A. Bredikhina, D. V. Zakharychev, F. S. Akhatova, D. B. Krivolapov, I. A. Litvinov

A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation

Abstract: Both enantiomers of 1,2-epoxy-3-(2-cyanophenoxy)propane 1a were obtained and converted into enantiomeric bunitrolol hydrochlorides 3 to confirm the configuration of the formers; racemic 1a undergoes spontaneous resolution upon crystallization and could be resolved into individual enantiomers by a preferential crystallization with low efficiency.

Language: English

DOI: 10.1070/MC2006v016n05ABEH002388



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