Bioorganic and Medicinal Chemistry Letters p. 2945 - 2948 (1998)
Update date:2022-08-05
Topics:
Matsumoto, Naoki
Iinuma, Hironobu
Sawa, Tsutomu
Takeuchi, Tomio
Anti-rheumatic agent (±)-epoxyquinomicin B was synthesized for a 22% overall yield in eight steps from commercially available 3-hydroxy-4- nitrobenzaldehyde via the intermediate quinone 6 prepared by selective phenol oxidation of 5 by use of Fremy's salt as the key step.
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Doi:10.1016/S0040-4020(98)00995-8
(1998)Doi:10.1016/S0040-4020(99)00794-2
(1999)Doi:10.1016/j.bmcl.2003.12.101
(2004)Doi:10.1039/a808267g
(1998)Doi:10.1021/om980747m
(1999)Doi:10.1021/jo9814748
(1999)