Organic Letters · 2021 · 20 citations · 32 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsMacrocycle SynthesisOrganic SynthesisRetrosynthetic AnalysisAlkylation ProcessesAlkylation ReactionsCarbazole ChemistryCarbazole SynthesisHeterocycle FunctionalizationIndole ChemistryIndole SynthesisRing-forming Reactions
An alkylation/olefination cascade of indolecarboxaldehydes and phosphonate-functionalized donor–acceptor cyclopropanes affords functionalized dihydrocarbazoles and cyclohepta[cd]indoles in formal (3 + 3) and (4 + 3) cycloadditions. A minor modification to the reaction conditions also allows access to the fully aromatic heterocyclic scaffolds by thermal loss of an electron-rich aryl moiety.
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Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
Minoru Ishikura, Takumi Abe, Tominari Choshi et al. · Natural Product Reports · 2015 · 246 citations
Asymmetric Annulation of Donor–Acceptor Cyclopropanes with Dienes
Hao Xu, Jiang‐Lin Hu, Lijia Wang et al. · Journal of the American Chemical Society · 2015 · 205 citations