Phenol Oxidation and Biostnthesis.Part XII. Stereochemical Studies Related to the Biosynthesis Of the Morphine Alkaloids

Barton, D H R; Bhakuni, D S; James, R; Kirby, G W

dc.contributor.author	Barton, D H R
dc.contributor.author	Bhakuni, D S
dc.contributor.author	James, R
dc.contributor.author	Kirby, G W
dc.date.accessioned	2010-03-10T09:36:47Z
dc.date.available	2010-03-10T09:36:47Z
dc.date.issued	1967
dc.identifier.citation	Journal of Chemical Society (C), 1967, 128	en
dc.identifier.uri	http://hdl.handle.net/123456789/529
dc.description.abstract	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.	en
dc.format.extent	1652226 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.subject	Glyceric acids	en
dc.subject	Morphine precursor	en
dc.subject	Phenyl Oxidation	en
dc.subject	Biosynthesis	en
dc.title	Phenol Oxidation and Biostnthesis.Part XII. Stereochemical Studies Related to the Biosynthesis Of the Morphine Alkaloids	en
dc.type	Article	en