Phenol Oxidation and Biostnthesis.Part XII. Stereochemical Studies Related to the Biosynthesis Of the Morphine Alkaloids
IR@CDRI: CSIR-Central Drug Research Institute, Lucknow
View Archive Info| Field | Value | |
| Creator |
Barton, D H R
Bhakuni, D S James, R Kirby, G W |
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| Date |
2010-03-10T09:36:47Z
2010-03-10T09:36:47Z 1967 |
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| Identifier |
Journal of Chemical Society (C), 1967, 128
http://hdl.handle.net/123456789/529 |
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| 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.
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| Format |
1652226 bytes
application/pdf |
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| Language |
en
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| Subject |
Glyceric acids
Morphine precursor Phenyl Oxidation Biosynthesis |
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| Title |
Phenol Oxidation and Biostnthesis.Part XII. Stereochemical Studies Related to the Biosynthesis Of the Morphine Alkaloids
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| Type |
Article
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