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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
5
|
| pubmed:dateCreated |
1995-10-24
|
| pubmed:abstractText |
The photochemical hypoiodination of cortisol acetonide gave a mixture of 18-iodocortisol acetonide and of the 11 beta,19-oxidoderivative. The proportion of the two products was slightly modified by the reaction temperature. Deprotection of the acetonide group of the 11 beta,19-oxidoderivative gave 11 beta,19-oxido-17 alpha,21-dihydroxy-4-pregnen-3,20-dione which led to the formation of 11 beta,19-oxido-4-androsten-3,17-dione upon treatment with sodium bismutate.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
May
|
| pubmed:issn |
0039-128X
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
60
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
411-3
|
| pubmed:dateRevised |
2000-12-18
|
| pubmed:meshHeading |
pubmed-meshheading:7570715-Androstenedione,
pubmed-meshheading:7570715-Chromatography, Thin Layer,
pubmed-meshheading:7570715-Hydrocortisone,
pubmed-meshheading:7570715-Iodine,
pubmed-meshheading:7570715-Magnetic Resonance Spectroscopy,
pubmed-meshheading:7570715-Models, Chemical,
pubmed-meshheading:7570715-Molecular Structure,
pubmed-meshheading:7570715-Oxidants, Photochemical,
pubmed-meshheading:7570715-Temperature
|
| pubmed:year |
1995
|
| pubmed:articleTitle |
A simple synthesis of 11,19-oxidosteroids.
|
| pubmed:affiliation |
Laboratoire de biologie hormonale, Hôpital Saint Louis, Paris, France.
|
| pubmed:publicationType |
Journal Article
|