Total Synthesis of (+)-Phrymarolin I from (+)-Malic Acid

(+)-Phrymarolin I was stereoselectively synthesized from (R)-(+)-3-hydroxybutanolide that had been prepared from (+)-malic acid. The procedure is more efficient than our previous synthesis in terms of fewer reaction steps and the easier availability of the starting material.

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Veröffentlicht in:Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 1997, Vol.61 (4), p.660-663
Hauptverfasser: Okazaki, Momotoshi, Ishibashi, Fumito, Shuto, Yoshihiro, Taniguchi, Eiji
Format: Artikel
Sprache:eng
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Zusammenfassung:(+)-Phrymarolin I was stereoselectively synthesized from (R)-(+)-3-hydroxybutanolide that had been prepared from (+)-malic acid. The procedure is more efficient than our previous synthesis in terms of fewer reaction steps and the easier availability of the starting material.
ISSN:0916-8451
1347-6947
DOI:10.1271/bbb.61.660