Tetrahedron Letters p. 7003 - 7006 (1999)
Update date:2022-07-30
Topics:
Rudas, Monika
Nyerges, Miklos
Toeke, Laszlo
Pete, Bela
Groundwater, Paul W.
Acridone 8 was prepared by the nucleophilic addition of aniline 4 to benzyne 5. Hydrolysis of the ester group, followed by cyclisation gave the acridone 8, which was subsequently converted to the pyrano[3,2-b]acridin-4-ones 11 and 17.
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Doi:10.1021/ja992583m
(1999)Doi:10.1016/j.ejmech.2017.07.077
(2017)Doi:10.1021/jo0110092
(2002)Doi:10.1002/ejoc.201300389
(2013)Doi:10.1248/cpb.47.1322
(1999)Doi:10.1021/jm991085l
(1999)
