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Berger, U. ; Burgemeister, T. ; Dannhardt, G. ; Mayer, K. K. ; Wiegrebe, Wolfgang

A Novel Approach to 4-Benzylisoquinolines

Berger, U., Burgemeister, T., Dannhardt, G., Mayer, K. K. and Wiegrebe, Wolfgang (1984) A Novel Approach to 4-Benzylisoquinolines. Tetrahedron 40 (1), pp. 215-220.

Date of publication of this fulltext: 01 Jul 2010 08:55
Article
DOI to cite this document: 10.5283/epub.15629


Abstract

The reaction of quinone methides with 3.4-dihydroisoquinoline or isoquinoline leads to benzylisoquinoline derivatives. NMR and ms investigations als well as chemical degradation prove that benzylation takes place at C-4 of the isoquinoline nucleus. Spectroscopic data are given for all new compounds.


Involved Institutions


Details

Item typeArticle
Journal or Publication TitleTetrahedron
Publisher:Elsevier
Volume:40
Number of Issue or Book Chapter:1
Page Range:pp. 215-220
Date1984
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-156293
Item ID15629

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