Journal of the Chemical Society. Perkin transactions I p. 1213 - 1218 (1996)
Update date:2022-07-30
Topics: Synthesis X-ray structure Inverto-yuehchukene 10-(indol-3′-yl) isomer (4aRS,10aRS)-1,1,3-trimethyl-1,2,4a,5,10,10a-hexahydroindene[1,2-b]indol-10-one
Cheng, Kin-Fai
Cheung, Man-Ki
A total synthesis of inverto-yuehchukene 4 and its 10-(indo-3′-yl) isomer 7 is described. The key tetracyclic ketone intermediate 13 was synthesized by a coupling reaction between 3-indolylzinc reagent and acid chloride 11, followed by Nazarov cyclization
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