Journal of Antibiotics p. 624 - 630 (1996)
Update date:2022-08-10
Topics:
Kogen, Hiroshi
Tago, Keiko
Kaneko, Satoru
Hamano, Kiyoshi
Onodera, Kaori
Haruyama, Hideyuki
Minagawa, Katsuhiro
Kinoshita, Takeshi
Ishikawa, Tomio
Tanimoto, Tatsuo
Tsujita, Yoshio
Schizostatin (1) has been isolated as a potent and selective inhibitor of squalene synthase. Its structure has been determined using spectroscopic methods: the compound is shown to be a diterpenoid which has a trans-dicarboxylic acid moiety. Total synthesis of schizostatin (1) was achieved by the highly regio- and stereoselective coupling reaction of an allylic bromide with a barium reagent. The Z-isomer 16 was also prepared using the stereoselective syn-addition of an organocopper reagent to acetylenedicarboxylate.
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