Journal of the Chemical Society. Chemical communications p. 114 - 115 (1981)
Update date:2022-08-05
Topics:
Iida, Hideo
Yuasa, Yoshifumi
Kibayashi, Chihiro
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.
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Doi:10.1016/S0040-4039(01)90282-5
(1981)Doi:10.1039/c9gc04191e
(2020)Doi:10.1007/BF00949662
(1980)Doi:10.1021/om0496434
(2004)Doi:10.1016/0040-4039(81)80121-9
(1981)Doi:10.1021/jm00345a003
(1982)
