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Stereospezifische Synthese zweier 9,11,12,12,13a,14- Hexahydro-dibenzo(f,h)pyrrolo(1,2-b)isochinoline

Faber, L. and Wiegrebe, Wolfgang (1976) Stereospezifische Synthese zweier 9,11,12,12,13a,14- Hexahydro-dibenzo(f,h)pyrrolo(1,2-b)isochinoline. Helvetica Chimica Acta 59 (6), pp. 2201-2212.

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Date of publication of this fulltext: 22 Jun 2010 06:23

Abstract

Summary. The stereospecific synthesis of (13aS)-( + )-2,3,6- and 3,4,6-
trimethoxy-9,11,12,13,13a, 14-hexahydrodibenzo[/, A]pyrrolo[l, 2-&]isoquinoline is described. The
2,3,6-trimethoxy-compound proved to be the optical antipode of (— )-antofine, isolated from
Cynanchum vincetoxicum L. Pers.


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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:15451
Owner only: item control page

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