Abstract
2,3-Dimethylindole (1) reacts by tin(II)chloride catalysis with arylaldehydes in dichloromethane, which contains 0.2% ethanol, regioselectively to the indol-1-yl-aryl-ethoxy-methanes3 a, 3 b.
Literatur
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Pindur, U., Schiffl, E. Regioselektive Zinn(II)chlorid-induzierte N-Aralkoxy-alkylierung am 2,3-Dimethylindol. Monatsh Chem 117, 1461–1463 (1986). https://doi.org/10.1007/BF00810754
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DOI: https://doi.org/10.1007/BF00810754