The structure of the orange pigment from Pseudomonas aureofaciens. The biogenesis of strychnine. Beckman fission of a gamma-keto oxime
PART I. The structure of the orange pigment from Pseudomonas aureofaciens was investigated and found to be 1-carboxy-2-hydroxyphenazine. A degradation product, 1-methyl-2-methoxyphenazine, was shown to be identical to a synthetic sample. PART II. The biogenesis of the indole alkaloid, strychnine...
| Summary: | PART I.
The structure of the orange pigment from Pseudomonas aureofaciens was investigated and found to be 1-carboxy-2-hydroxyphenazine. A degradation product, 1-methyl-2-methoxyphenazine, was shown to be identical to a synthetic sample.
PART II.
The biogenesis of the indole alkaloid, strychnine, was studied by administration of C[superscript 14] labelled precursors to Strychnos nus-vomica plants and degradations of the radioactive strychnine isolated from the plants. The results indicate an acetate origin for the non-tryptophan portion and a formate origin for the "berberine bridge" carbon of strychnine.
PART III.
A Beckmann fission of the tosylate of the [gamma]-keto oxime, 3-acetoxylanostane-7, 11-dione-7-oxime, was carried out with sodium t-butoxide, and the expected cleavage of ring B and formation of a nitrile and unsaturated ketone occurred.
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