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Total Synthesis of the Dimeric Cephalotaxus Alkaloid (-)-Cephalancetine C
Peng-Zhen Sheng1, Zhi-Bin Ni2,1, Jia-Hui Zhao2,1
1State Key Laboratory of Phytochemistry and Natural Medicines, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming650201, China.
Abstract:
Cephalancetine C, a prototype of the dimeric Cephalotaxus alkaloids, was first synthesized in the laboratory via a convergent two-segment approach. Key steps included an aldol reaction and a stereospecific 5-exo-trig aza-Michael addition. This strategy was developed after an unsuccessful attempt to pursue a biomimetic pathway in which a Polonovski-type reaction of 7 unexpectedly produced conjugated cyclic enamine 8.
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