473980-85-7Relevant academic research and scientific papers
Stereoselective synthesis of the styryllactones, 7-epi-goniodiol and leiocarpin A, isolated from Goniothalamus leiocarpus
Chen, Jian,Lin, Guo-Qiang,Liu, Han-Quan
, p. 8111 - 8113 (2007/10/03)
Two novel styryllactones, 7-epi-goniodiol and leiocarpin A, isolated from Goniothalamus leiocarpus, were stereoselectively synthesized in a short and efficient route from cinnamyl alcohol based on the asymmetric epoxidation and the palladium-catalyzed cross-coupling of vinyl epoxide with vinyltributylstannane.
A short and general approach to the synthesis of styryllactones: (+)-Goniodiol, its acetates and β-trifluoromethyl derivative, (+)-7-epi-Goniodiol and (+)-9-deoxygoniopypyrone
Chen, Jian,Lin, Guo-Qiang,Wang, Zhi-Min,Liu, Han-Quan
, p. 1265 - 1268 (2007/10/03)
(+)-Goniodiol, its acetates and β-trifluoromethyl derivative, (+)-7-epi-Goniodiol and (+)-9-deoxygoniopypyrone, the representatives of styryllactones have been synthesized in a short and general way. The key steps involve the regioselective asymmetric dihydroxylation and the palladium-catalyzed cross-coupling of cyclic allylic carbonate with vinyltributylstannane.
