Phytochemistry p. 945 - 948 (1980)
Update date:2022-08-05
Topics:
Rastogi, Kamesh
Kapil, Randhir S.
Popli, Satya P.
Chemical investigation of the roots of G. mauritiana resulted in the isolation of two new alkaloids; 1-hydroxy-3-methoxy-2-(3-methylbut-2-enyl)-N-methylacridan-9-one (1) and 4,8-dimethoxy-3-(3-methylbut-2-enyl)-N-methyl-2-quinolone (6). The structures of these new bases have been established by chemical and spectroscopic methods and confirmed in the case of 6 by its synthesis. Interestingly, the formic acid-catalysed cyclisation of 1 gave the dealkylated product 3 along with the pyrano-[2, 3-a]-acridine (4).
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Doi:10.1002/ejic.201600417
(2016)Doi:10.1246/bcsj.53.2275
(1980)Doi:10.1021/jo01049a031
(1962)Doi:10.1021/jo00315a034
(1981)Doi:10.1021/ja049805n
(2004)Doi:10.1021/ja073573l
(2007)
