1979
DOI: 10.1002/jlcr.2580160418
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Marquage de la Pregnenolone au Carbjne 14 et au Deuterium en Position 21

Abstract: NOTE "IQUAGE DE LA PFEGNENOLONE AU CAPBINE 14 FT AU DEUTERIUM EN POSITION 21 S W Y 5 Pregnenolone ( A -pregnen-3B-ol-20-one) is labelled with 14C and deuterium in position 21. The radioactive carbon is inserted by the means of diazomethane-14C. The deuteration is realized by the reduction of 21-diazo-pregnenolone under the action of iodhydric acid dissolved in D20.14 C et le chlorure de l'acide 6ti6nioue ac6tyl6 4. Signalons Outre la rn6thode utilis6e par PHILLAMY et SCHOLZ, au rroins tmis autres possibilit6s … Show more

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Cited by 3 publications
(1 citation statement)
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“…Acyl halides and anhydrides form diazoketones, which upon treatment with HCl or HBr furnish a-haloketones, whereas HI reduces them to methyl ketones 148 . Aldehydes and cyclic ketones give fairly good yields of methyl ketones and ring-expanded homologs, respectively.…”
Section: Reactions At the Methylene Groupmentioning
confidence: 99%
“…Acyl halides and anhydrides form diazoketones, which upon treatment with HCl or HBr furnish a-haloketones, whereas HI reduces them to methyl ketones 148 . Aldehydes and cyclic ketones give fairly good yields of methyl ketones and ring-expanded homologs, respectively.…”
Section: Reactions At the Methylene Groupmentioning
confidence: 99%