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Syntheses of Anthracenones, 1. Sodium Dithionite Reduction of peri-Substituted Anthracenediones

Prinz, H., Wiegrebe, Wolfgang and Müller, K. (1996) Syntheses of Anthracenones, 1. Sodium Dithionite Reduction of peri-Substituted Anthracenediones. The Journal of Organic Chemistry 61 (8), pp. 2853-2856.

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Abstract

The reaction of peri-substituted anthracenediones with sodium dithionite in dimethylformamide and water has been investigated. The system selectively reduces the carbonyl group flanked by the peri substituents of the anthracenediones to give the corresponding 4,5-disubstituted 9(10H)-anthracenones and thus provides a route to anthracenones which are otherwise difficult to obtain. Many functional ...

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Item type:Article
Date:1996
Institutions:Chemistry and Pharmacy > Institute of Pharmacy > Alumni or Retired Professors > Prof. Wiegrebe
Interdisciplinary Subject Network:Not selected
Identification Number:
ValueType
10.1021/jo9520351DOI
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:15912
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