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2.two]decane Main and defining the geometry from the exocyclic double bond. The activation energies of formation of the vinyl-gold intermediates had been calculated and revealed a silyl enol ether having an unprotected indole moiety as an acceptable precursor for the Toste cyclization. This six-move synthesis didn't require any nonstrategic redox m
two.2]decane core and defining the geometry from the exocyclic double bond. The activation energies of formation of the vinyl-gold intermediates have been calculated and exposed a silyl enol ether with the unprotected indole moiety as an appropriate precursor to the Toste cyclization. This six-action synthesis didn't include any nonstrategic redox
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