## Abstract 5β[4,5β^13^C~2~]β and 5β[1,5β^13^C~2~]Aminolevulinic acid (ALA) have been synthesized by the Gabriel condensation of potassium phthalimide with ethyl bromo[1,2β^13^C~2~]acetate (derived from [1,2β^13^C~2~]acetic acid) or ethyl bromo[2β^13^C]βacetate (derived from sodium [2β^13^C]acetate
Synthesis of 4-thia[5-13C]lysine
β Scribed by Amarendra Nath Maity; Shyue-Chu Ke
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- French
- Weight
- 150 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
This report describes the synthesis of 4βthia[5β^13^C]lysine, an isotopomer of 4βthialysine that is an analog of lysine. It was synthesized from 2βamino[1β^13^C]ethanol hydrochloride (1) in two steps. In the first step, 1 was converted to 2βbromo[2β^13^C]ethylamine hydrobromide (2). The reaction of cysteine with 2 in basic condition followed by acidification afforded 4βthia[5β^13^C]lysine hydrochloride (3).
π SIMILAR VOLUMES
## Abstract New synthetic routes were developed for incorporating ^13^C into the oxazaphosphorine ring and nitrogen mustard functionality of cyclophosphamide metabolites. 1,2β^13^C~2~βVinylbromide and ethylene oxide were used to synthesize 3,4β^13^C~2~β3βbutenyl N,Nβbis(2βchloroethyl)phosphorodiami
Carbonylation of 1-undecene with 13C0 under a hydrogen atmosphere with pa 1 ladi um-s tannous ch 1 or ide cata 1 ys t afforded [ 1-13C Idodecanoi c ( 1 aur i c acid on a 0.25 mole scale. Reduction to the alcohol and treatment with concentrated HBr gave 1-[l-C]bromododecane which was used to alkylate