The conjugated methyl e s t e r s o f chenodeoxycholic 15 and c h o l i c 23 a c i d s a r e t h e key i n t e r m e d i a t e s t o these syntheses.
Labeled bile acids V: Deuterium and carbon-13 labeled cholic, chenodeoxycholic and ursodeoxycholic acids
β Scribed by Chee Kong Lai; Chang Yon Byon; Marcel Gut; Danuta Mostowicz; Warren G. Anderson
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- French
- Weight
- 364 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
This paper describes a general, simple and short procedure for the introduction o f stable isotopes (deuterium and carbon-13) to the side chain of bile acids. The bisnorcholyl aldehydes of cholic and chenodeoxycholic acids are key intermediates, while the isotope is introduced by the Wittig condensation o f [1 ,2-13 C2]-(carbethoxyrnethylene)triphenylphosphorane.
π SIMILAR VOLUMES
## Abstract A series of 5Ξ²βcholanic acids labeled with deuterium in the A ring were prepared by exchange labeling of the corresponding ketone by column chromatography on deuterated alumina. Factors affecting yield and labeling efficiency are discussed. 5Ξ²βCholanic acids labeled with ^13^C in the ca
## Abstract Valproic acid and sodium valproate labeled with carbonβ14 in the 2βposition were synthesized. Deuterium labeled valproic acid was also synthesized and the extent of deuterium incorporation was determined by several analytical methods.