Alkaloids of Corydalis incisa PERS. V. The structures of corydalispirone and corydalisol.

Chemical and Pharmaceutical Bulletin
1975.0

Abstract

Two new alkaloids, corydalispirone, C₂₀H₁₇O₆N, mp 196-198°, [α]D 0°, and corydalisol, C₂₀H₂₁O₅N, mp 160-161°, [α]D +21.4°, were isolated from Corydalis incisa PERS. (Papaveraceae). The structure of corydalispirone was established to be I by the spectroscopic examinations and chemical correlation with bicucullinediol and adlumidinediol, and the structure of corydalisol was determined as VIII by the conversion to d-tetrahydrocoptisine. Corydalispirone and corydalisol are noted as a new series of isoquinoline-type alkaloids having one more carbon atom at the benzyl moiety, and probably are metabolites of coptisine.

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