Publication | Open Access
Direct Functionalization of (Un)protected Tetrahydroisoquinoline and Isochroman under Iron and Copper Catalysis: Two Metals, Two Mechanisms
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Citations
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References
2011
Year
Inorganic ChemistryChemical EngineeringNovel OrganocatalystsEngineeringDirect FunctionalizationCopper CatalysisOrganic ChemistryOrganometallic CatalysisCatalysisMolecular CatalysisChemistryIron CatalystsSimple CopperHeterocycle ChemistrySynthetic ChemistryBiomolecular EngineeringNatural Product Synthesis
A highly facile, straightforward synthesis of 1-(3-indolyl)-tetrahydroisoquinolines was developed using either simple copper or iron catalysts. N-protected and unprotected tetrahydroisoquinolines (THIQ) could be used as starting materials. Extension of the substrate scope of the pronucleophile from indoles to pyrroles and electron-rich arenes was realized. Additionally, methoxyphenylation is not limited to THIQ but can be carried out on isochroman as well, again employing iron and copper catalysis.
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