The alkaloids of the genus Datura, section Brugmansia. V. Alkaloids of D. sanguinea R. and P. and related esters of tropane-3 alpha, 6-beta, 7 beta-triol.
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Alkaloids↗
Biomedical subjects
W C Evans
Publications and source records attributed to W C Evans.
Dissimilation of aromatic substrates by Rhodopseudomonas palustris.
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Acetates↗
The alkaloids of the genus Datura, section Brugmansia. IV. New alkaloids of D. sanguinea R. and P.
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Atropa belladonna↗
The alkaloids of Datura meteloides D.C.
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Alkaloids↗
The alkaloids of the genus Datura, section Brugmansia. 3. Datura sanguinea R. and P.
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Alkaloids↗
Oxidative metabolism of naphthalene by soil pseudomonads. The ring-fission mechanism.
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Aldehydes↗
Oxidative metabolism of phthalic acid by soil pseudomonads.
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Journal Article↗
Oxidation of phenol and benzoic acid by some soil bacteria.
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Bacteria↗
The 'tryptophanase-tryptophan reaction: Possible mechanisms for the inhibition of indole production by glucose in cultures of B. coli.
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Journal Article↗
The tryptophanase-indole reaction: Some observations on the production of tryptophanase by Esch. coli; in particular the effect of the presence of glucose and amino acids on the formation of tryptophanase.
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Journal Article↗
A comparative study of the production of l-3:4-dihydroxyphenylalanine from tyrosine by tyrosinase from various sources.
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Journal Article↗
The accumulation of l-3:4-dihydroxyphenylalanine in the tyrosinase-tyrosine reaction.
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Journal Article↗
The comparative phytochemistry of the genus Erythroxylon.
Recent research suggests that, in addition to the well-documented occurrence of significant quantities of cocaine and related alkaloids in a limited number of species, the genus Erythroxylon will prove to be a rich source of tropane alkaloids. These bases are esters of a range of acids with tropine, 3 alpha, 6 beta-dihydroxytropane and 3 alpha, 6 beta, 7 beta-trihydroxytropane; the numbers are further increased by nor-derivatives, and stereoisomerism involving the C-3 hydroxyl of the tropane skeleton. The diterpenes of the genus also appear worthy of further study.
Alkaloids↗