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RESEARCH PRODUCT
Reactions of 1-isopropyl-3-methyl- and 2,3-dimethylindoles with triethyl orthoformate: New trisindolylmethanes
Ulf PindurJohann Müllersubject
Steric effectschemistry.chemical_compoundchemistryBicyclic moleculeOrganic ChemistryStructural isomerOrganic chemistryOrthoesterNuclear magnetic resonance spectroscopyTriethyl orthoformateIsopropyldescription
Indoles 1 and 2 react with triethyl orthoformate under proton–catalyzed conditions to form trisindolylmethanes. The regioisomer distribution of the products is controlled by steric and electronic factors.
year | journal | country | edition | language |
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1987-01-01 | Journal of Heterocyclic Chemistry |