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2.2]decane core and defining the geometry with the exocyclic double bond. The activation energies of formation on the vinyl-gold intermediates were being calculated and exposed a silyl enol ether with the unprotected indole moiety as an appropriate precursor to the Toste cyclization. This 6-phase synthesis did not entail any nonstrategic redox mani
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two.two]decane core and defining the geometry in the exocyclic double bond. The activation energies of formation from the vinyl-gold intermediates had been calculated and unveiled a silyl enol ether by having an unprotected indole moiety as an acceptable precursor for that Toste cyclization. This six-move synthesis did not involve any nonstrategic