52744-22-6Relevant articles and documents
Wari et al.
, p. 5955 (1975)
A Novel Synthesis of (+)-4-Demethoxydaunomycinone
Cabri, Walter,De Bernardinis, Silvia,Francalanci, Franco,Penco, Sergio
, p. 428 - 429 (1990)
(+)-4-Demethoxydaunomycinone (2) was obtained in five steps through the selective formation of the trifluormethanesulphonate (4) and its palladium-catalysed reduction.
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
Cameron, Donald W.,Feutrill, Geoffrey I.,Griffiths, Peter G.
, p. 25 - 40 (2007/10/03)
Hydrogenation of the anthracyclines daunorubicin (1) and doxorubicin (2) gave selective deoxygenation at position 5. Hydride reduction of (1) and (2) gave complementary regiocontrol, leading to 12-deoxygenation or 5,12-bisdeoxygenation. This chemistry all
Synthesis and biological activity of (R)-2'-fluorocarminomycin
Baer,Hernandez Mateo
, p. 2055 - 2059 (2007/10/02)
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