255. Der sterische Verlauf der Gyclisierung von β-(Cyclohexen-(l)-yl)-äthylaminen zu 10-Hydroxy-decahydroisochinolinen Decahydroisochinoline, III. Teil-Reference-Cited by-同舟云学术

255. Der sterische Verlauf der Gyclisierung von β-(Cyclohexen-(l)-yl)-äthylaminen zu 10-Hydroxy-decahydroisochinolinen Decahydroisochinoline, III. Teil

Published:1966 Issue:7 Volume:49 Page:2175-2189
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:en
Short-container-title:Helv. Chim. Acta

Author:

Grob C. A.,Wohl R. A.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference41 articles.

1. 254. Die säurekatalysierte Isomerisierung von 10-Hydroxy-N-methyl-cis-decahydroisochinolin. Herstellung von N-Methyl-Δ9′ 10-octahydroisochinolin Decahydroisochinoline. II. Teil [1]

2. Die Darstellung von Oktahydro-isochinolin-Derivaten durch Ringschluß

3. Isochinolin-Derivate Mit Oxyd-Brücken

4. Vgl. R. A. Wohl, Dissertation, Universität Basel 1965.

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