162600-01-3Relevant articles and documents
Julia-Colonna asymmetric epoxidation of furyl styryl ketone as a route to intermediates to naturally-occurring styryl lactones
Chen, Wei-Ping,Roberts, Stanley M.
, p. 103 - 105 (2007/10/03)
The enone 1 was oxidized stereoselectively using urea-hydrogen peroxide with polyleucine as the catalyst to give the epoxide 2 which was used to make (+)-goniotriol 7, (+)-goniofufurone 8, (+)-8-acetylgoniotriol 9 and goniopypyrone 10.
Asymmetric Total Synthesis of (+)-Goniotriol and (+)-Goniofufurone
Yang, Zhi-cai,Zhou, Wei-shan
, p. 1429 - 1436 (2007/10/02)
Thr Enantioselective synthesis of two antitumor styryl lactones, (+)-goniotriol and (+)-goniofufurone, have been completed starting from cinnamyl alcohol in ten and eleven steps with an overall yield of 21percent and 12percent, respectively.
Total synthesis of the natural goniodiol-8-monoacetate from cinnamyl alcohol
Yang,Zhou
, p. 743 - 744 (2007/10/02)
The first total synthesis of goniodiol-8-monoacetate, using the Sharpless asymmetric epoxidation starting from cinnamyl alcohol in twelve steps with an overall yield of 7%, is achieved.
