## Abstract (lβ^14^C)βdodecanal was synthesized from (lβ^14^C)βdodecanoic acid. The twoβstep synthesis beginning with 0.9 mg of the acid resulted in an overall yield of 42 % after purification. The final product was separated from the starting material and side products by silicic acid column chrom
A method for preparing small quantities of 14C-labeled staphylococcal enterotoxin B
β Scribed by John P. Bowden
- Book ID
- 118309061
- Publisher
- Elsevier Science
- Year
- 1968
- Weight
- 224 KB
- Volume
- 168
- Category
- Article
- ISSN
- 0005-2795
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A thod is described for the preparation of 5-bromopentanoic--5 & acid which is inserted the Wittig ylid into the desired prostaglandin intermediate in the 1 ast carbon-carbon bond forming step of the Corey synthesis. Thr diffe nt prostaglandins were prepared carbon-labeled (both pgC and i5Q in the m