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|Title:||Phenol Oxidation and Biostnthesis.Part XII. Stereochemical Studies Related to the Biosynthesis Of the Morphine Alkaloids|
|Authors:||Barton, D H R;Bhakuni, D S;James, R;Kirby, G W|
|subject:||Glyceric acids;Morphine precursor;Phenyl Oxidation;Biosynthesis|
|Description:||Ozonolysis of tritiated Salutaridinols-I and-II has afforded glyceric acids whose absolute confiurations have been determined by the isotope dilution method.In this way the stereochemistry of salutaridinol-I, the Precursor of the morphine alakaloids, has been defined unambiguosly.|
|Standard no:||Journal of Chemical Society (C), 1967, 128|
|Appears in Collections:||Medicinal and Process Chemistry|
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