Concise assembly of the polycyclic frameworks associated with the hapalindole and fischerindole alkaloids
Martin G Banwell1, Xinghua Ma, Rebecca M Taylor
1Research School of Chemistry, Australian National University, Canberra, ACT 0200, Australia. mgb@rcs.anu.edu.au
Abstract:
[reaction: see text] Reaction of N-methylindole (4) with 6,6-dibromobicyclo[3.1.0]hexane (5) in the presence of silver tetrafluoroborate affords conjugate 7 in 67% yield. This product can be readily elaborated to compounds 12b and 13b which embody the polycyclic frameworks associated with members of the hapalindole and fischerindole classes of alkaloids. The chiral-auxiliary-substituted 6,6-dibromobicyclo[3.1.0]hexanes 21 and 22 react with indole to give adducts likely to be useful in the enantioselective total synthesis of the title alkaloids.
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