Tetrahedron Letters p. 1481 - 1484 (1982)
Update date:2022-08-02
Topics:
Masaki, Yukio
Hashimoto, Kinji
Sakuma, Kazuhiko
Kaji, Kenji
The ochtodane skeleton is formed stereoselectively from myrcene via acid-catalyzed cyclization of the benzenesulfenyl chloride adduct and the epoxide in a biogenetic type fashion.Its application to the syntheses of two ochtodane-type monoterpenes, an aldehyde component of the boll weevil pheromone and a diol found in the red alga Ochtodes crockeri, is reported.
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Doi:10.1021/ol006301v
(2000)Doi:10.1021/om049773c
(2004)Doi:10.1016/j.jinorgbio.2015.05.014
(2015)Doi:10.1248/cpb.31.683
(1983)Doi:10.1021/jo00142a008
(1982)Doi:10.1021/ja01214a060
(1946)
