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Removal of the Pyrrolidine Group by Dehydrogenation of a 4-Pyrrolidin-2-yl-tetrahydroisoquinoline

Mahboobi, Siavosh, Seidl, E., Eibler, E. and Wiegrebe, Wolfgang (1992) Removal of the Pyrrolidine Group by Dehydrogenation of a 4-Pyrrolidin-2-yl-tetrahydroisoquinoline. Archiv der Pharmazie 325, pp. 679-683.

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Date of publication of this fulltext: 12 Jul 2010 07:40

Abstract

Dehydrogenation of 6,7-dimethoxy-1-methyl-4-(N-methyl-pyrrolidin-2-yl)-3,4-dihydroisoquinoline (9) by Pd/C in tetraline leads to dehydrogenated products, rearrangement, and elimination of the pyrrolidine group mainly as N-methylpyrrolidine (Scheme 3). Die Dehydrierung von 6,7-Dimethoxy-1-methyl-4-(N-methyl-pyrrolidin-2- yl)-3,4-dihydroisochinolin (9) mit Pd/C in Tetralin führt zu ...

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Item type:Article
Date:1992
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:15776
Owner only: item control page

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