Carbon-13 nuclear magnetic resonance spectral assignments of grayanotoxin-I.

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The 13C-NMR signals of grayanotoxin-I, a tetracyclic diterpene with an A-nor-B-homo-ent-kaurane skeleton, were assigned by means of single-frequency off-resonance decoupling, selective proton decoupling and by comparison with spectra of derivatives.

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