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3,10-Dimethoxyprotoberberines

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

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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.

Item Type:Article
Institutions: Chemistry and Pharmacy > Institute of Pharmacy > Retired Professors > Prof. Wiegrebe
Subjects:500 Science > 540 Chemistry & allied sciences
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Unknown
Owner:Universitätsbibliothek Regensburg
Deposited On:07 Jul 2010 07:06
Last Modified:21 Jul 2011 00:32
Item ID:15669
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