Issue 1, 1999

Convenient syntheses of cyclic carbazole oligomers by 1-pot Knoevenagel reaction

Abstract

Syntheses of cyclic carbazole oligomers by a 1-pot Knoevenagel reaction without using high dilution methods are described. Cyclic carbazole oligomers of several ring sizes could be obtained in high yields when 3,6-diformyl-9-docosylcarbazole and appropriate aromatic compounds having a bis(cyanoacetate) group were reacted in THF using DMAP as a base at 40 °C.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1999, 41-46

Convenient syntheses of cyclic carbazole oligomers by 1-pot Knoevenagel reaction

S. Maruyama, Y. Zhang, T. Wada and H. Sasabe, J. Chem. Soc., Perkin Trans. 1, 1999, 41 DOI: 10.1039/A807158F

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