The syntheses of all the possible 2 H , 1 3 C , and 15N singly and multigly labelled isotopomers of acetonitrile and thioacetamide are described. The pathway includes reaction between methyl iodide and potassium cyanide followed by treatment of the acetonitrile with diphenylphosphinodithioic acid to
Synthesis and characterisation of 13C and 15N isotopomers of a 1-acyl-7-nitroindoline
β Scribed by John E. T. Corrie; Andreas Barth; George Papageorgiou
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- French
- Weight
- 106 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.494
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β¦ Synopsis
Abstract
Efficient methods are described for synthesis of isotopomers of the waterβsoluble, photolabile 1βacylβ7βnitroindoline 5 with either ^13^C in the carbonyl of the acyl substituent or ^15^N in the nitro group. The isotopic incorporations were verified by IR difference spectroscopy coupled with flash photolysis.
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