1970•Journal of the Chemical Society C OrganicRequires access

The alkaloids of Corydalis pallida var. tenuis (Yatabe) and the structures of pallidine and kikemanine

Tetsuji Kametani, Manabu Ihara, Takashi Honda

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Abstract

Separation of the alkaloids from Corydalis pallida var. tenuis (Yatabe) afforded the known alkaloids, (–)-tetrahydropalmatine, protopine, capaurine, capaurimine, (+)-isoboldine, sinoacutine, and kikemanine (the last-named was identical with corydalmine), and the previously unknown alkaloids, pallidine and ‘alkaloid P.’ The morphinandienone alkaloid, pallidine, was also identified as (+)-isosalutaridine, the racemate of which has been synthesised previously.

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Separation of the alkaloids from Corydalis pallida var. tenuis (Yatabe) afforded the known alkaloids, (–)-tetrahydropalmatine, protopine, capaurine, capaurimine, (+)-isoboldine, sinoacutine, and kikemanine (the last-named was identical with corydalmine), and the previously unknown alkaloids, pallidine and ‘alkaloid P.’ The morphinandienone alkaloid, pallidine, was also identified as (+)-isosalutaridine, the racemate of which has been synthesised previously.

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Available abstract

Separation of the alkaloids from Corydalis pallida var. tenuis (Yatabe) afforded the known alkaloids, (–)-tetrahydropalmatine, protopine, capaurine, capaurimine, (+)-isoboldine, sinoacutine, and kikemanine (the last-named was identical with corydalmine), and the previously unknown alkaloids, pallidine and ‘alkaloid P.’ The morphinandienone alkaloid, pallidine, was also identified as (+)-isosalutaridine, the racemate of which has been synthesised previously.

Key concepts: Protopine, Corydalis, Tetrahydropalmatine, Alkaloid, Sanguinarine, Papaveraceae, Botany, Biology

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