骨化三醇 、
(12R)-acetoxyoleic acid 在
N,N'-二环己基碳二亚胺 、
4-二甲氨基吡啶 作用下,
以
四氢呋喃 、
二氯甲烷 为溶剂,
反应 14.25h,
生成 (1R,3S,Z)-3-hydroxy-5-(2-((1R,3aS,7aR,E)-1-((R)-6-hydroxy-6-methylheptan-2-yl)-7a-methyloctahydro-4H-inden-4-ylidene)ethylidene)-4-methylenecyclohexyl (R,Z)-12-acetoxyoctadec-9-enoate 、 (1S,5R,Z)-5-hydroxy-3-(2-((1R,3aS,7aR,E)-1-((R)-6-hydroxy-6-methylheptan-2-yl)-7a-methyloctahydro-4H-inden-4-ylidene)ethylidene)-2-methylenecyclohexyl (R,Z)-12-acetoxyoctadec-9-enoate