Publication | Closed Access
Synthesis of C3-Alkylated Indoles on DNA via Indolyl Alcohol Formation Followed by Metal-Free Transfer Hydrogenation
27
Citations
36
References
2019
Year
Combinatorial ChemistryBioorganic ChemistryEngineeringOrganic ChemistryChemistryChemical DerivativeC3-alkylated IndolesMedicinal ChemistryLibrary CompoundsIndolyl Alcohol FormationMetal-free Transfer Hydrogenation3-Alkylated Indole CoresCatalysisSynthesis MethodNatural Product SynthesisBiomolecular EngineeringNatural SciencesDerivative (Chemistry)Synthetic Chemistry
3-Alkylated indole cores have been found in countless natural products and many biologically active compounds, including pharmaceuticals. In this report, a highly efficient approach to C3-alkylated indole derivatives on DNA via indolyl alcohol formation followed by metal-free transfer hydrogenation is developed. This on-DNA C3 alkylation approach is attractive because library compounds can be constructed from simple aldehydes or acid functionalized aldehydes, which are widely commercially available.
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