The total synthesis of 13(R)- and 13(S)-dihydro-4-demethoxy-daunorubicin. Revision of stereochemistry of the microbial and mammalian reduction product of 4-demethoxydaunorubicin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
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1. New Chiral Pool Approach to Anthracyclinones. The Stereoselective Synthesis of Idarubicinone;The Journal of Organic Chemistry;2003-02-20
2. 5-Deoxy, 12-Deoxy, 5,12-Bisdeoxy, and 4,5,12-Trisdeoxy Anthracyclines: Synthesis of New Analogues of Daunorubicin and Doxorubicin by Controlled Deoxygenation of the C-Ring.;Australian Journal of Chemistry;2000
3. Stereoselectivity of idarubicin reduction in various animal species and humans;Xenobiotica;1991-01
4. Reductive transformations of 10-deoxydaunomycinone;The Journal of Organic Chemistry;1990-04
5. Improved antitumor effects of 3'-deamino-3'-morpholino derivatives of pirarubicin.;The Journal of Antibiotics;1990
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