Synthesis of a potent rhodomycin, oxaunomycin, and its analogs

DOI: 10.1248/cpb.40.61

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 61 - 65 (1992)

Update date:2022-08-02

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Authors:

Kita Kita

Maeda Maeda

Kirahara

Fujii Fujii

Nakajima

Yamamoto

Tamura Tamura

Fujioka Fujioka

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Article abstract of DOI:10.1248/cpb.40.61

Oxaunomycin (3) and its regioisomer (6) were synthesized by employing regioselective glycosidations of the C-7 hydroxyl group of 10-O-acetyl-β-rhodomycinone (16) and the C-10 hydroxyl group of the C-7,9-O-phenylboronate (14), respectively, in the presence

Full text of DOI:10.1248/cpb.40.61

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