Publication | Closed Access
Catalytic asymmetric C2-nucleophilic substitutions of C3-substituted indoles with ortho-hydroxybenzyl alcohols
45
Citations
55
References
2017
Year
High YieldsEngineeringOrtho-hydroxybenzyl AlcoholsNatural SciencesDiversity-oriented SynthesisC3-substituted IndolesCatalytic SynthesisTriaryl Methane ProductsOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Catalytic asymmetric C2-nucleophilic substitutions of C3-substituted indoles such as tryptophols or tryptamines with <italic>ortho</italic>-hydroxybenzyl alcohols have been established, leading to the generation of triaryl methane products in generally high yields and excellent enantioselectivities.
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