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Non-hemiterpenoid Quinolines

Non-hemiterpenoid Quinolines.—A re-examination of the alkaloids of Haplophyllum dubium resulted in the isolation of two members of the 2-aryl-4-quinolone group, i.e. graveoline (2 R = Me) and the new alkaloid norgraveoline (2 R = H).5 A new bacterial pseudan (3) has been obtained from Pseudomonas aeruginosa.8 [Pg.71]

Yajima, N. Kato, and K. Munakata, Agric. Biol. Chem., 1977, 41, 1263. [Pg.71]

Mester, J. Reisch, K. Szendrei, and J. Korosi, Liebigs Ann. Chem. 1979, 1785. [Pg.71]


Non-hemiterpenoid Quinolines.—New sources of the simple quinolines 4-methoxy-l-methyl-2-quinolone and its 8-methoxy-derivative (folimine) have been reported the former was isolated from Myrtopsis sellingii9 and from Zanthoxylum cuspidatum,16 and folimine was shown to be a constituent of Haplophyllum perforatum.5 The latter species also contains foliosidine (9), previously isolated from H. foliosum. The micro-organism Pseudomonas aertiginosa has been shown to contain 2-(hept-l-enyl)-4-quinolone (12).10 The structure of the alkaloid was established by n.m.r. and mass spectroscopy and by its synthesis from aniline and the j3-keto-ester Me(CH2)4CH=CHC0CH2C02Me. [Pg.80]

Non-hemiterpenoid Quinolines.—The three non-hemiterpenoid quinoline alkaloids reported this year are all 3-metho iyquinoline derivatives. Furoquinoline alkaloids had been isolated previously from Chloroxylon swietenia (East Indian satin wood), but now two new alkaloids, swietenidins A and B, have been obtained from the bark. Spectroscopic studies of swietenidin A and its monomethyl ether, and comparison of the data with those of the known 8-methoxy-iV-methyl-2-quinolone lunacridine, indicated that the alkaloid was the... [Pg.78]


See other pages where Non-hemiterpenoid Quinolines is mentioned: [Pg.287]    [Pg.81]    [Pg.76]    [Pg.287]    [Pg.287]    [Pg.81]    [Pg.76]    [Pg.287]    [Pg.86]   


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Hemiterpenoids

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