Die Reaktion des 2,3,4a,8a-Tetrachlor-6,7-dimethyl-4a,5,8,8a-tetrahydro-1,4-naphthochinons mit Aminen
Fachrichtung Pharmazeutische Chemie der Universität des Saarlandes, Postfach 11 50, D-66041 Saarbrücken
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Author to whom correspondence should be addressed.
Sci. Pharm. 2000, 68(2), 129-139; https://doi.org/10.3797/scipharm.aut-00-12
Submission received: 19 October 1999
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Revised: 13 December 1999
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Accepted: 13 December 1999
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Published: 1 April 2000
Abstract
2,3,4a,8a-Tetrachloro-6,7-dimethyl-4a,5 ,8,8a-tetrahydro-1,4-naphthoquinone (5) reacts with arylamines 8a-e to give 2-amino-dihydroquinones 4a-e. Alkylamines 8f and h give 2-amino-dihydroquinones 4f, h and 2-amino-1,4-naphthoquinones 7f, h, dialkylamines 9f, g, i and j give 2-amino-dihydroqulnones 3f, g, i, j, 2-amino-1,4-naphthoquinones 6f, g, i, j and the photodesalkylated products 10f and g.
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MDPI and ACS Style
Kallmayer, H.-J.; Doerr, M. Die Reaktion des 2,3,4a,8a-Tetrachlor-6,7-dimethyl-4a,5,8,8a-tetrahydro-1,4-naphthochinons mit Aminen. Sci. Pharm. 2000, 68, 129-139. https://doi.org/10.3797/scipharm.aut-00-12
AMA Style
Kallmayer H-J, Doerr M. Die Reaktion des 2,3,4a,8a-Tetrachlor-6,7-dimethyl-4a,5,8,8a-tetrahydro-1,4-naphthochinons mit Aminen. Scientia Pharmaceutica. 2000; 68(2):129-139. https://doi.org/10.3797/scipharm.aut-00-12
Chicago/Turabian StyleKallmayer, H.-J., and M. Doerr. 2000. "Die Reaktion des 2,3,4a,8a-Tetrachlor-6,7-dimethyl-4a,5,8,8a-tetrahydro-1,4-naphthochinons mit Aminen" Scientia Pharmaceutica 68, no. 2: 129-139. https://doi.org/10.3797/scipharm.aut-00-12
