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1294 alkaloids arranged in alphabetical order t with details of their producing plants and of the structure, composition, and melting points of the alkaloids and their derivatives, specific rotations, solubilities, spectral characteristics (UV, IR, PMR, 13C NMR, etc.), information on pharmacology, and references to original papers and to unpublished investigations. UV spectra were taken in ethanol (kma x, nm; log c); IR spectra, as a rule, for molded tablets with KBr (cm-1), and 1H and 13C NMR spectra in deuterochloroform (6 scale, ppm, values of J in Hz), except where otherwise mentioned.Abbreviations of the literature sources encountered most frequently are given in Chapter 1 of this review.Conventional symbols and abbreviations used in the review:{ } --the melting points of characteristic derivatives are given within braces;

on Chroma~on N-AW, at i column temperature o~ 202°C and ~ p=aao~ra o~ ~h~ =a==i~ ~6 (hsllum) o~ 0,7 kg~/cm', and also a 1,2 m ~ 3 mm column ~illed wi~h ~% SE-30 on Chroma~ou N-AW at a column =empera~ure of 220°C and a hellum prsosure of 0.65 kg£/c~ i. 0n the polar phase, the by-product issued as a slngle peak with methyl palmitate, exaggerating i~s true amount, and on the nonpolar phase i~ was eluted together with the solvent.

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