Issue 3, 1981

A one-step synthesis of acridines via palladium(II)-catalysed ring formation of allylated enaminones

Abstract

9-Ethyl-3,4,5,6,9,10-hexahydroacridine-1(2H),-8(7H)-dione (5) and its N-allyl analogue (6) were formed in a one-step ring-forming reaction from both the 2-and/or N-allyl derivatives of 3-aminocyclohex-2-enone (1)–(4) and from the bisenaminone (7), obtained from the N-allylenaminone (2), on treatment with PdCl2(MeCN)2.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 114-115

A one-step synthesis of acridines via palladium(II)-catalysed ring formation of allylated enaminones

H. Iida, Y. Yuasa and C. Kibayashi, J. Chem. Soc., Chem. Commun., 1981, 114 DOI: 10.1039/C39810000114

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