Abstract
Several alkaloids are postulated to be derived from anthranilic acid. These include some rather simple substituted anthranilic acids, quinolines, and some with condensed ring systems of various types. Some of the parent nuclei of these alkaloids are as follows:
Excellent herbs had our fathers of old —
Excellent herbs to ease their pain —
Alexanders and Marigold,
Eyebright, Orris, and Elecampane —
Basil, Rocket, Valerian, Rue,
(Almost singing themselves they run)
Vervain, Dittany, Call-me-to-you —
Cowslip, Melilot, Rose of the Sun.
Our Fathers of Old, Rudyard Kipling*
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Bibliography
Leete, E., L. Marion, and I. D. Spenser: Can. J. Chem. 33, 405–410 (1955).
Leete, E., L. Marion, and I. D. Spenser: Chem. Ind. (London) 1957, 1270.
Munsche, D., and K. Mothes: Phytochem. 4, 705–712 (1965).
Nair, P. M., and C. S. Vaidyanathan: Phytochem. 3, 513–523 (1964).
Vishin, M. L., D. Munsche und H.-B. Schröter: Flora (Jena) 154, 299–316 (1964).
Boit, H.-G.: Ergebnisse der Alkaloid-Chemie bis 1960. Berlin: Akademie Verlag 1961.
Monkovie, I., I. D. Spenser, and A. O. Plunkett: Can. J. Chem. 45, 1935–1948 (1967).
Matsuo, M., M. Yamazaki, and Y. Kasida: Biochem. Biophys. Res. Communs. 23, 679–682 (1966).
Aneja, R., S. K. Mukerjee, and T. R. Seshadri: Tetrahedron 4, 256–270 (1958).
Luckner, M.: Europ. J. Biochem. 2, 74–78 (1967).
Baldwin, M. E., I. R. Bilk, A. A. Komzak, and J. R. Price: Tetrahedron 16, 206–211 (1961).
Eliasberg, J., P. Friedländer: Ber. deut. chem. Ges. 25, 1752–1760 (1892).
Fitzgerald, J. S., S. R. Johns, J. A. Lamberton, and A. H. Redcliffe. Australian J. Chem. 19, 151–159 (1966).
Gröger, D., S. Johne und K. Monhes: Experientia 21, 13–14 (1965).
Skursky, L.: Collection Czechoslov. Chem. Communs. 30, 2080–2083 (1965).
Robinson, T.: Phytochem. 4, 67–74 (1965).
Yamazaki, M., A. Ikuta, T. Mori, and T. Kawana: Tetrahedron Letters 1967, 3317–3320.
Prager, R. H., and G. R. Skurray: Australian J. Chem. 21, 1037–1042 (1968). Anthranilic acid-3,5-3H and mevalonic acid-2-14C fed to Acronychia baueri gave rise to labelled acronidine.
Cobet, M., and M. Luckner: Europ. J. Biochem. 4, 76–78 (1968). 2,4-dihydroxyquinoline-3-14C fed to Ruta graveolens gave rise to labelled kokusaginine. The precursor exists in pH-dependent equilibrium with 2-aminobenzoyl acetic acid
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 1968 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Robinson, T. (1968). Quinolines and Other Alkaloids Related to Anthranilic Acid. In: The Biochemistry of Alkaloids. Molecular Biology Biochemistry and Biophysics / Molekularbiologie Biochemie und Biophysik, vol 3. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-01015-0_11
Download citation
DOI: https://doi.org/10.1007/978-3-662-01015-0_11
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-04275-4
Online ISBN: 978-3-662-01015-0
eBook Packages: Springer Book Archive