Total Synthesis of the Sesterterpenoid (+/-)-Palauolide

DOI: 10.1039/c39870001342

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1342 - 1343 (1987)

Update date:2022-08-04

Topics: Yield NMR spectroscopy Catalyst Stereochemistry Chromatography Total synthesis Chemical Synthesis Isoprene unit

Authors:

Piers, Edward

Wai, John S. M.

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Article abstract of DOI:10.1039/c39870001342

Transformation of 3,6-dimethylcyclohex-2-enone (2) into the sesterterpenoid (+/-)-palauolide (1) was accomplished via a 17-step sequence of reactions.

Full text of DOI:10.1039/c39870001342

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