Please use this identifier to cite or link to this item: http://dl.umsu.ac.ir/handle/Hannan/23063
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
Year: 1967
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.
URI: http://hdl.handle.net/123456789/529
Standard no: Journal of Chemical Society (C), 1967, 128
Appears in Collections:Medicinal and Process Chemistry

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