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two.2]decane core and defining the geometry on the exocyclic double bond. The activation energies of development of the vinyl-gold intermediates were calculated and disclosed a silyl enol ether with the unprotected indole moiety as an acceptable precursor to the Toste cyclization. This six-move synthesis did not entail any nonstrategic redox manipu
2.2]decane core and defining the geometry from the exocyclic double bond. The activation energies of formation from the vinyl-gold intermediates were being calculated and revealed a silyl enol ether with an unprotected indole moiety as a suitable precursor for that Toste cyclization. This six-step synthesis didn't contain any nonstrategic redox man