Synthesis of aminated naphthacenetriones: Precursors to aminated anthracyclines

Article abstract of DOI:10.1080/00397919308011183

An application of aminoacetaldehyde dialkoxy acetal to introduce an amino fuctionality in the 6 and/or 11 position of the naphthacenetrione ring system, resulting in key intermediates to aminated anthracyclines, is described.

Full text of DOI:10.1080/00397919308011183

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Synthesis of Aminated
Naphthacenetriones:
Precursors to Aminated
Anthracyclines
Manik S. Sardessai a , Hanley N. Abramson a & Henry
C. Wormser a
a Department of Pharmaceutical Sciences , College
of Pharmacy and Allied Health Professions Wayne
State University , Detroit, Michigan, 48202
Published online: 23 Sep 2006.
To cite this article: Manik S. Sardessai , Hanley N. Abramson & Henry C. Wormser
(1993) Synthesis of Aminated Naphthacenetriones: Precursors to Aminated
Anthracyclines, Synthetic Communications: An International Journal for Rapid
Communication of Synthetic Organic Chemistry, 23:22, 3223-3229
To link to this article: http://dx.doi.org/10.1080/00397919308011183
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