Journal of the Chemical Society. Chemical communications p. 500 - 502 (1988)
Update date:2022-07-29
Topics: Diels-Alder Reaction Experimental terms Aqueous Formal total synthesis
Brandes, Ellen
Grieco, Paul A.
Garner, Philip
A formal synthesis of the Inhoffen-Lythgoe diol (1) featuring a novel intermolecular Diels-Alder strategy wherein an intact C(20) stereocentre as part of a unit is used to elaborate directly the stereocentres at C(13) and C(17) of the hydrindan ring syste
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