Synthesis of inverto-yuehchukene and its 10-(indol-3′-yl) isomer. X-Ray structure of (4aRS,10aRS)-1,1,3-trimethyl-1,2,4a,5,10,10a-hexahydroindene[1,2-b]indol-10-one

DOI: 10.1039/P19960001213

Source and publish data:

Journal of the Chemical Society. Perkin transactions I p. 1213 - 1218 (1996)

Update date:2022-07-30

Topics: Synthesis X-ray structure

Authors:

Cheng, Kin-Fai

Cheung, Man-Ki

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Article abstract of DOI:10.1039/P19960001213

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

Full text of DOI:10.1039/P19960001213

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