By R.H.F Manske, H.L. Holmes
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Extra resources for Alkaloids: Chemistry and Pharmacology: v. 11
169. M. Koch, M. Plat, B. C. Das, and J. Le Men, Tetrahedron Letters 2353 (1966). 170. P. Brauchli, V. Deulofeu, H. Budzikiewicz, and C. Djerassi, J . A m . Chem. 86, 1895 (1964); H. Monteiro, H. Budzikiewicz, C. Djerassi, R. R. Arndt, and W. H. Baarschers, Chem. Commun. 317 (1965). 170a. S. R. Johns, J. A. Lamberton, and J. L. Occolowitz, Chem. Commun. 229 (1967). 171. P. Potier, C. Kan, J. -M. Janot, H. Budzikiewicz, and C. Djerassi, Bull. Soc. Chim. France 2309 (1966); J. Le Men, C. Kan, P. -M.
Sci. 93, 597 (1964); C A 63, 12003b (1965). 159. F. Fish and F. Newcombe, J. Pharm. Pharmacol. 16, 832 (1964). 160. A. T. McPhail and G. A. Sim, J. Chem. Soc. 1663 (1965). 161. A. R. Battersby and D. A. Yeowell, J. Chem. 4419 (1964). 162. H. Muller, M. Hesse, P. Waser, H. Schmid, and P. Karrer, Helv. Chim. Acta 48, 320 (1965). 163. J. S. Grossert, J. M. Hugo, M. E. von Klemperer, and F. L. Warren, J. Chem SOC. 2812 and 2814 (1965). 164. N. G. Bisset, Chem. & Ind. (London) 1036 (1965); J. L. Occolowitz, K.
The principal new carbon-nitrogen networks belong t o the sarpagine subgroup (Chart I),the important ones being the 3,4- and 4,21-seco-l0-deoxysarpagineskeletons, which are also found as components of the voacanga and alstonia dimeric alkaloids, respectively. , burnamicine, picraphylline (Table IV). The 3,4-secosarpagines are often found along with their sarpagine equivalents ; a t our present level of understanding of biosynthesis it is not known if such 2-acylindoles are intermediates in the formation of, or are derived from, their ring-closed equivalents (2).
Alkaloids: Chemistry and Pharmacology: v. 11 by R.H.F Manske, H.L. Holmes