By J R Hanson; James Ralph Hanson; Royal Society of Chemistry (Great Britain); et al
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Additional resources for A review of the literature published between September 1975 & August 1976
Brasil. , 1975,83, 131 763). W. -J. Schneider, and H . Schneider-Bernohr, Annalen, 1975, 1690. -C. Jacquesy, R. -F. Patoiseau, Terrahedron, 1976, 32, 1699. N. Kitagawa, M. Nojima, and N. S. 5; X = OH) and Table 1 refers to CO instead of C 0 2 . R. Antkowiak and W. Z . Antkowiak, Bull. A c a d . polon. , Sir. Sci. , 1976, 24. 291; the corresponding ketone may have been formed by Bardyshev as ketone X, I. I . , V. Kosnikova, A. L. Pertsovskii, and L. M. Krezo, Doklady A k a d . , 1969,186, 1325 (Chem.
R. D. Henson, D. L. Bull, R. L. Ridgway, and G. W. Ivie, J. Agric. , 1576, 24, 228. B. Matai and R. M. Sathe, J. Inorg. , 1976,38, 1748. B. Frei and H. R. Wolf, Helv. Chim. Acta, 1976, 59, 82. P. C. Traas, H. Boelens, and H. J. Takken, Rec. Trav. , 1976, 95, 57. P. C. Traas, H. Boelens, and H. J. Takken, Tetrahedron Letters, 1976, 2287. K. C. Rice and R. S. Wilson, J. Medicin. , 1976, 19, 1054. C. Fournier, D. Paquer, and M. Vazeux, Bull. chim. France, 1975, 2753; cf. Vol. 4, p. 60 for the unquoted synthesis of thioverbenone.
I. Souzu and H. Mitsuhashi, Tetrahedron Letters, 1969, 2725. 271 Further papers on the more complex monoterpenoid alkaloids lie outside the scope of this Report; the reader is referred to the Specialist Periodical Reports on the Alkaloids. Further work on secoiridoid biosynthesis has now shown, using [7,EL3H2]-7deoxyloganic acid, that the C-8 proton as well as the C-7 proton is retained in the sequence loganin -+ secologanin (126) -+ morroniside (129) (cf. Vol. 3, p. 28) in Lonicera morrowii, Cornus officinalis, and Gentiana t h ~ n b e r g i i .