Publication | Open Access
General and Efficient Synthesis of Indoles through Triazene‐Directed C–H Annulation
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2013
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Excellent RegioselectivityChemical EngineeringExperimental SynthesisTriazene‐directed C–h AnnulationEngineeringBiochemistryNatural SciencesDiversity-oriented SynthesisOrganic ChemistryCatalysisChemistryTitle MethodSynthesis MethodNatural Product SynthesisSynthetic ChemistryBiomolecular EngineeringRhodium Migration
Unprotected indoles are prepared with the title method, which has a wide scope for alkynes. Excellent regioselectivity was accomplished for aryl–alkyl and alkyl–alkyl disubstituted acetylenes. This reaction features an unusual 1,2 rhodium migration and ring-contraction-triggered NN bond cleavage. It allows rapid conversion of the reaction products into several functional molecules. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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