330438-05-6Relevant articles and documents
First enantioselective total synthesis of (-)-13-hydroxyneocembrene
Liu, Zuosheng,Zhang, Tao,Li, Yulin
, p. 275 - 277 (2001)
The first enantioselective total synthesis of (-)-13-hydroxyneocembrene (1), a naturally occurring cembranoids isolated from soft coral Sarcophyton trocheliophorum, was achieved via a general approach by employing intramolecular McMurry coupling as a key step from (S)-(+)-carvone.
First total synthesis and absolute configuration of (-)-13-hydroxy-11,12-epoxy-neocembrene
Zhang,Liu,Li
, p. 393 - 398 (2007/10/03)
The first enantioselective total synthesis of (-)-13-hydroxy-11,12-epoxy-neocembrene (1), a naturally occurring cembranoid isolated from soft coral Sarcophyton trocheliophorum, was achieved via a general approach by employing intramolecular McMurry coupling as a key step from (S)-(+)-carvone. The absolute configuration of the epoxide function of 1 is concluded as (11S, 12S).