Synthesis and characterization of [1-14C]N-methylneodecanamide
✍ Scribed by A. Charig; K. Kinscherf; B. Gariullo; S. Roman; T. F. Connors; C. Unkefer; I. T. Horvath
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- French
- Weight
- 226 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0022-2135
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📜 SIMILAR VOLUMES
therefore been incorporated in this isoprenoid. The
Methyl bromoacetate was reacted with trimethyla~nine-[~'C] dissolved in methanol, forming the methyl ester of [I4C] labeled betaine hydrobromide. The methyl ester was hydrolyzed in an alkaline medium to (carboxymethy1)trimethylammonium hydroxide inner salt, and then transformed into the hydrochlorid
1-(1'-[14C1-2',3'-Dideoxy-~-~glyceropent-2'-enofuranosy~~thymine (1'-114C1-d4T), was synthesized kom l-[14Cl-ribose, 1, in 7 steps in an overall yield of 29.3%. 1-[14C]-Ribose was converted in one step to l-O-methy1-2,3,5-tri-O-benzoylribofuranoside 2 in quantitative yield. Compound 2 was converted