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Weimar, C. ; Angerer, S. von ; Wiegrebe, Wolfgang

Synthesis of C-13-Alkylated 8-oxoberberbines

Weimar, C., Angerer, S. von and Wiegrebe, Wolfgang (1991) Synthesis of C-13-Alkylated 8-oxoberberbines. Archiv der Pharmazie 324, pp. 907-912.

Date of publication of this fulltext: 08 Jul 2010 05:11
Article
DOI to cite this document: 10.5283/epub.15733


Abstract

C-13-alkylated methoxy-8H-dibenzo[a,g]quinolizin-8-ones 2a-e were synthesized by photocyclization of 1 -alkylidene-N-benzoyl-1,2,3,4-tetrahydroisoquinolines 1. Moreover, condensation of 1,2,3,4-tetrahydro-6,7-dimethoxy- 1-oxo-isoquinoline with homophthalic acid anhydrides 7a and b leads to the C-13-alkylated 8-oxoberbines 2b and c and improves the yields compared with those of the ...

C-13-alkylated methoxy-8H-dibenzo[a,g]quinolizin-8-ones 2a-e were synthesized
by photocyclization of 1 -alkylidene-N-benzoyl-1,2,3,4-tetrahydroisoquinolines
1. Moreover, condensation of 1,2,3,4-tetrahydro-6,7-dimethoxy-
1-oxo-isoquinoline with homophthalic acid anhydrides 7a and b leads to
the C-13-alkylated 8-oxoberbines 2b and c and improves the yields compared
with those of the photocyclization method.

Die C-13-alkylierten Methoxy-8H-dibenzo[a,g]chinolizin-8-one 2a-e wurden
durch Photozyklisierung der 1-Alkyliden-N-benzoyl-1,2,3,4-tetrahydroisochinoline
1 synthetisiert, aber auch die Kondensation von 1,2,3,4-Tetrahydro-
6,7-dimethoxy-1-oxo-isochinolin mit den Homophthalsäureanhydriden
7a und b führt zu den C-13-alkylierten 8-Oxoberbinen 2b und c und verbessert
die Ausbeuten, verglichen mit der Photozyklisierungsmethode.


Involved Institutions


Details

Item typeArticle
Journal or Publication TitleArchiv der Pharmazie
Publisher:John Wiley & Sons
Volume:324
Page Range:pp. 907-912
Date1991
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-157339
Item ID15733

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