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Extra resources for Carotenoids℃5. Contributed Papers Presented at the Fifth International Symposium on Carotenoids Madison, Wisconsin, USA, 23–28 July 1978
This shortcoming befalls not only this but also numerous other works. Particularly for such rare and difficultly accessible carotenoids, that is very regrettable. In section 4, I will go into more detail about chiriquixanthin A (11) and B (12), isolated from the skin of a frog. As derivatives of ε,ε-carotene they both offer particular interest. The possible identity with the so-called tunaxanthin (from fish) is still not definitely clarified. A very significant and in many ways also instructive structure revision has ari sen for the hydroxycarotenoids 2JL a n d M · * have put the old suggestions in brackets next to the new ones.
Milas, Science 103, 581-583 (1946). 0. Isler, W. Huber, A. Ronco and M. Kofler, Helv. Chim. Acta 30, 1911-1927 (1947); 0. Isler, A. Ronco, W. Guex, N. C. Hindley, W. Huber, K. Dialer and M. Kofler, Helv. Chim. Acta 32, 489-505 (1949); H. Lindlar, Helv. Chim. Acta 35, 446-450 (1952). D. A. van Dorp and J. F. Arens, Nature (London) 160, 189 (1947); J. F. Arens and D. A. van Dorp, Reel. Trav. Chim. Pays-Bas 68, 604-608 (1949). J. D. Cawley, C. D. , 112th Meet. Am. Chem. S o c , New York (1947); 0.
Rep. , No. 557, Geneva (1974). U. Manz and 0. Isler, in Kosmetika, Riechstoffe, Lebensmittelzusatzstoffe (edited by H. Aebi, E. Baumgartner, H. Fiedler and G. Ohloff), Georg Thieme, Stuttgart (in press). Commission on the European Communities, Ref. , 1975). Symposium: Utilization of Plant Pigments, Food Technol. (Chicago) 29, 37-54 (May 1975). Pure & Appi. , Vol. 51, pp. 463-506, Pergamon Press Ltd. 1979. Printed in Great Britain. CHARACTERISATION, CHEMISTRY AND STEREOCHEMISTRY OF CAROTENOIDS Conrad Hans Eugster Institute of Organic Chemistry, University of Zurich, Ramistrasse 76, CH-8001 Zurich, Switzerland Abstract - A review is presented on progress made since the 4th International Symposium on Carotenoids, Berne, Switzerland, 1975» in the following areas of carotenoid chemistry: - New structures.