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Acylcyclopropanes are employed as useful donor-acceptor cyclopropanes that undergo formal (4 + 2) cyclocondensation with N-unprotected 3-substituted indoles in the presence of a Brønsted acid catalyst. The reaction involves the simultaneous alkylation of both the N and C-2 positions of the indole and provides access to the 8,9-dihydropyrido[1,2-a]indole scaffold that is the central core of several biologically relevant indole alkaloids in excellent yields and good selectivities.
acylcyclopropanes, brønsted acid catalyzed, donor−acceptor cyclopropanes, (4 + 2) cyclocondensation, 540
acylcyclopropanes, brønsted acid catalyzed, donor−acceptor cyclopropanes, (4 + 2) cyclocondensation, 540
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