
Bioorganic and Medicinal Chemistry Letters p. 2033 - 2036 (1997)
Update date:2022-08-04
Topics:
Nakamura, Shizuo
Goto, Kiyoto
Kondo, Mitsuyoshi
Naito, Shinsaku
Tsuda, Yoshiaki
Shishido, Kozo
A practical and enantioselective total synthesis of the mercapturic acid sulfoxide 4, a metabolite of anti-inflammatory drug DUP 697 1, has been accomplished by employing the substrate-controlled diastereoselective oxidation of the sulfide 7 to the sulfoxide 8 as the key step. This led to the structure determination of 4.
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Doi:10.1007/BF00908457
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