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Abbaureaktionen an 3-(2'-(2"Dimethylaminoäthyl)-phenyl)iso-chromanen

Wiegrebe, Wolfgang, Stephan, H.M., Fricke, J. and Schlunegger, U.P. (1976) Abbaureaktionen an 3-(2'-(2"Dimethylaminoäthyl)-phenyl)iso-chromanen. Helvetica Chimica Acta 59 (3), pp. 949-962.

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Date of publication of this fulltext: 22 Jun 2010 06:22

Abstract

Summary:
Degradation of the /?-dimethylaminoethyl sidechain of properly substituted 3-aryl-isochromanes
produce inter alia the amines 2, the styrenes 3, the aldehyde 5b and the carboxylic acid 4b.
The racemates of the amine 15 and the aldehyd 5b were resolved; the chiral center of the
menthoxycarbonyl-hydrazone was eliminated b y ester interchange.


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Item type:Article
Date:1976
Institutions:Chemistry and Pharmacy > Institute of Pharmacy > Alumni or Retired Professors > Prof. Wiegrebe
Dewey Decimal Classification:500 Science > 540 Chemistry & allied sciences
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Unknown
Item ID:15450
Owner only: item control page

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