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two.2]decane core and defining the geometry from the exocyclic double bond. The activation energies of development of the vinyl-gold intermediates were being calculated and disclosed a silyl enol ether having an unprotected indole moiety as an acceptable precursor to the Toste cyclization. This six-move synthesis didn't entail any nonstrategic redo

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2.two]decane core and defining the geometry on the exocyclic double bond. The activation energies of development with the vinyl-gold intermediates were being calculated and exposed a silyl enol ether with an unprotected indole moiety as a suitable precursor to the Toste cyclization. This 6-move synthesis didn't include any nonstrategic redox manipu

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