ChemInform Abstract: DIE CYANAETHYLIERUNG DER ISOMEREN DES 2,5‐DIMETHYLTETRAHYDROTHIOPYRANONS‐(4) UND DIE SELEKTIVE RED. DES 2,5‐DIMETHYL‐5‐(BETA‐CYANAETHYL)‐TETRAHYDROTHIOPYRANONS‐(4) UND ‐PIPERIDONS‐(4)

Sharifkanov, A. Sh.; Bushneva, N. A.; Tokmurzin, K. Kh.; Chanysheva, I. S.

doi:10.1002/chin.197219280

Chemischer Informationsdienst

1972

DOI: 10.1002/chin.197219280

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ChemInform Abstract: DIE CYANAETHYLIERUNG DER ISOMEREN DES 2,5‐DIMETHYLTETRAHYDROTHIOPYRANONS‐(4) UND DIE SELEKTIVE RED. DES 2,5‐DIMETHYL‐5‐(BETA‐CYANAETHYL)‐TETRAHYDROTHIOPYRANONS‐(4) UND ‐PIPERIDONS‐(4)

A. Sh. Sharifkanov¹,

N. A. Bushneva²,

K. Kh. Tokmurzin³

et al.

Abstract: Von den cis‐trans‐isomeren Thiopyranonen (I) und (II) läßt sich bei Zimmertemperatur in Gegenwart von Kaliumhydroxid in Äther nur die cis‐Verbindung (II) mit Acrylnitril (III) cyanäthylieren.

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ChemInform Abstract: DIE CYANAETHYLIERUNG DER ISOMEREN DES 2,5‐DIMETHYLTETRAHYDROTHIOPYRANONS‐(4) UND DIE SELEKTIVE RED. DES 2,5‐DIMETHYL‐5‐(BETA‐CYANAETHYL)‐TETRAHYDROTHIOPYRANONS‐(4) UND ‐PIPERIDONS‐(4)

Abstract: Von den cis‐trans‐isomeren Thiopyranonen (I) und (II) läßt sich bei Zimmertemperatur in Gegenwart von Kaliumhydroxid in Äther nur die cis‐Verbindung (II) mit Acrylnitril (III) cyanäthylieren.

This publication either has no citations yet, or we are still processing them

See others like this or search for similar articles

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