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Chinnasamy, P. ; Iwasa, K. ; Angerer, S. von ; Weimar, C. ; Wiegrebe, Wolfgang

3,10-Dimethoxyprotoberberines

Chinnasamy, P., Iwasa, K., Angerer, S. von, Weimar, C. and Wiegrebe, Wolfgang (1987) 3,10-Dimethoxyprotoberberines. Archiv der Pharmazie 320, pp. 790-798.

Date of publication of this fulltext: 07 Jul 2010 05:06
Article
DOI to cite this document: 10.5283/epub.15669


Abstract

Protoberberines with the unusual 3,10-dimethoxy substitution are synthesized by photocyclization of E- and
Z-1-ethylidene-1,2,3,4-tetrahydro-6-methoxy-2-(3-methoxybenzoyl)isoquinolines.

Protoberberine mit ungewöhnlicher 3,10-Dimethoxysubstitution werden durch Photocyclisierung von E -
und Z-l-Ethyliden-1,2,3,4-tetrahydro-6-methoxy-2-(3-methoxybenzoyl)-isochinolinen hergestellt.


Involved Institutions


Details

Item typeArticle
Journal or Publication TitleArchiv der Pharmazie
Publisher:John Wiley & Sons
Volume:320
Page Range:pp. 790-798
Date1987
InstitutionsChemistry and Pharmacy > Institute of Pharmacy > Alumni or Retired Professors > Prof. Wiegrebe
Dewey Decimal Classification500 Science > 540 Chemistry & allied sciences
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgUnknown
URN of the UB Regensburgurn:nbn:de:bvb:355-epub-156699
Item ID15669

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