2010
DOI: 10.1007/s10593-010-0488-z
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Synthesis of hydrogenated 2,7-dimethylpyrrolo[3,4-b]indoles – analogs of dimebon

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Cited by 16 publications
(11 citation statements)
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“…However, the spectrum of the (E)-isomer XII exhibited analogous resonances at 6.65 and 7.39 ppm with a much greater SSCC (14.8 Hz). Such values of the SSCC are characteristic of the discussed cis-and trans-isomers [14,18].…”
mentioning
confidence: 73%
“…However, the spectrum of the (E)-isomer XII exhibited analogous resonances at 6.65 and 7.39 ppm with a much greater SSCC (14.8 Hz). Such values of the SSCC are characteristic of the discussed cis-and trans-isomers [14,18].…”
mentioning
confidence: 73%
“…[14] Additionally,t hey are stable analogues of indole-2,3-quinodimethanesu sed for preparation of carbazoles,c arbolines,a nd related heterocyclic systems,t hrough cycloaddition reactions. [15,16] Moreover,t he pyrrolo [3,4-b]indole derivatives show ab road spectrum of pharmacological activity. [13] Although many methods for the construction of pyrrolo [3,4-b]indoles have been developed, ap reformed indole precursor is generally required.…”
mentioning
confidence: 99%
“…[6a] An exo'-selective enantioselective cyclization also has been achieved using a chiral IAP/Ni catalyst. [9,10] This strategy allows synthesis of pyrrolo [3,4-b]indole derivatives, [11,12] having a quaternary carbon center, which are structural isomers of cyclotryptamines. [9,10] This strategy allows synthesis of pyrrolo [3,4-b]indole derivatives, [11,12] having a quaternary carbon center, which are structural isomers of cyclotryptamines.…”
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confidence: 99%