z-logo
Premium
Synthesen in der Isochinolinreihe Halogensubstituierte 1‐(ω‐Phenylalkyl)‐1,2,3,4‐tetrahydro‐isochinoline als Analgetica
Author(s) -
Brossi A.,
Besendrof H.,
Pellmont B.,
Walter M.,
Schinder O.
Publication year - 1960
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19600430603
Subject(s) - chemistry , stereochemistry , medicinal chemistry , organic chemistry
Substituted 1‐methyl‐3,4‐dihydro‐isoquinolines can easily be converted to 2‐(β‐acylamido‐ethyl)‐acetophenomes. The latter have been used as intermediates for the synthesis of various substituted 1‐β‐phenylethyl‐2‐methyl‐1,2,3,4‐tetrahydro‐isoquinolines. Several of these compounds show interesting analgesic and spasmolytic properties, especially those containing a halogenated phenylethyl group.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom