Berberis alkaloids. XVII. Investigation of the alkaloids of Berberis heteropoda

The alkaloid composition of young shoots and leaves ofBerberis heteropoda Schrenk has been studied. In addition to known alkaloids, two new ones have been isolated — N-methyldihydroberberine and 8-oxoberberrubine, the structures of which were established by chemical transformations and a study of spectral properties. Of known alkaloids, berbamunine, aromoline, glaucine, thalicmidine, isocorydine, and reticuline have been found in this plant for the first time. Pseudopalmitine and laudanosine have been found for the first time in plants of the genusBerberis.Andizhan State Medical Institute. Institute of the Chemistry of Plant Substances of Uzbek Republic Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 53–59, January–February, 1993.     

Berberis alkaloids. XXVI. An investigation of the alkaloids ofBerberis amurensis

In addition to alkaloids isolated previously, young shoots of Berberis amurensis Rupr. have yielded berberrubine, oxyacanthine, and pseudopalmatine, and the new amorphous base amurenine. It's structure has been established on the basis of spectral characteristics and chemical transformations.     

Berberis alkaloids. XXIX. An investigation of the alkaloids ofBerberis sibirica

The alkaloid compositions of the roots, young shoots, and leaves of Berberis sibirica have been studied, and berberine, palmatine, columbamine, berberrubine, oxyacanthine, berbamine, 8-oxoberberine, 8-oxoberrberubine, pakistanine, and pronunciferine, and also the new base N-acetylhomoveratrylamine have been isolated. This is the first time that any of these alkaloids, except berberine, have been isolated from this plant. Andizhan State Medical Institute. Institute of the Chemistry of Plant Substances of the Academy of Sciences of the Uzbekistan Republic, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 424–428, May–June, 1993.     

Berberis alkaloids XXXIX. New alkaloids fromB. densiflora

The alkaloid composition of the leaves ofBerberis densiflora has been studied. Berberine, -allocryptopine. oxyacanthine, glaucine, thalicmidine, isocorydine, O-methylcorypalline and the new bases densinine and densiberine have been isolated. The structures of the new alkaloids have been established by a study of spectral characteristics and chemical transformations. This is the first time that any of the known alkaloids, apart from berberine, have been isolated from a plant of this pecies and it is the first time that -allocryptopine and O-methylcorypalline have been isolated from theBerberis genus.     

Berberis alkaloids. XXIX. An investigation of the alkaloids ofBerberis sibirica

The alkaloid compositions of the roots, young shoots, and leaves of Berberis sibirica have been studied, and berberine, palmatine, columbamine, berberrubine, oxyacanthine, berbamine, 8-oxoberberine, 8-oxoberrberubine, pakistanine, and pronunciferine, and also the new base N-acetylhomoveratrylamine have been isolated. This is the first time that any of these alkaloids, except berberine, have been isolated from this plant.Andizhan State Medical Institute. Institute of the Chemistry of Plant Substances of the Academy of Sciences of the Uzbekistan Republic, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 424–428, May–June, 1993.     

The synthesis of alkaloids of the ergotoxin group. 70. Section on ergot alkaloids

The syntheses of the alkaloids of the ergotoxine-group i.e. ergocristine, α- and β-ergokryptine, and ergocornine, are described. Using starting material with known stereochemistry these syntheses allowed to determine the absolute configurations also at C-2′ and C-12′ in the peptide part, which could not be derived from analytical data. All ergot alkaloids of the peptide type possess the same stereochemical structure.     

Berberis alkaloids XIV. Dynamics of the accumulation of alkaloids in Berberis oblonga

Andizhan State Medical Institute. Institute of Chemistry of Plant Substances, Uzbekistan Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 597–598, September–October, 1992.