A one-step synthesis of acridines via palladium(II)-catalysed ring formation of allylated enaminones
- 1 January 1981
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 3,p. 114-115
- https://doi.org/10.1039/c39810000114
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.Keywords
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