Issue 20, 1995

Stereocontrolled synthesis of indolo[2,3-a]quinolizines by intramolecular double Michael reaction: proof for stepwise mechanism

Abstract

Indolo[2,3-a]quinolizines 3 were stereoselectively synthesized by the intramolecular double Michael reaction of amide esters 2, the indole nitrogen of which was protected with a tosyl group, using ButMe2SiOSO2CF3 in the presence of Et3N.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 2085-2086

Stereocontrolled synthesis of indolo[2,3-a]quinolizines by intramolecular double Michael reaction: proof for stepwise mechanism

M. Ihara, Y. Ishida, Y. Tokunaga, C. Kabuto and K. Fukumoto, J. Chem. Soc., Chem. Commun., 1995, 2085 DOI: 10.1039/C39950002085

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