作者:Shigefumi Kuwahara、Masahiko Moriguchi、Kazuhiro Miyagawa、Masako Konno、Osamu Kodama
DOI:10.1016/0040-4020(95)00488-t
日期:1995.8
enantioselective synthesis of (−)-syringolides 1 and 2 which were isolated as specific elicitors produced by Pseudomonas syringae pv. tomato was accomplished in 11 steps from diethyl d tartrate. The specific rotations of synthetic samples were in good accord with those of the natural syringolides, and synthetic syringolide 2 showed almost the same biological activity as that of natural syringolide 2.
(-)-丁香油酸酯1和2的对映选择性合成,其作为丁香假单胞菌pv产生的特定引发剂被分离。从酒石酸二乙酯分11步完成番茄。合成样品的比旋光度与天然丁香酚的旋光度非常一致,合成丁香酚2的生物活性几乎与天然丁香酚2的生物活性相同。