作者:John E. T. Corrie、Gordon P. Reid
DOI:10.1002/jlcr.2580360312
日期:1995.3
[3-D]2-Nitroacetophenone and [alcohol-18O]-1-(2-nitrophenyl)ethyl alcohol were prepared and used to synthesise labelled P3-l-(2-nitrophenyl)ethyl esters of ATP (“caged ATP”) with isotope present either as deuterium on the 3-position of the nitrosubstituted ring or as 18oxygen in the bridging position between the terminal phosphate and the nitrophenylethyl group. The availability of the deuterated compounds enabled complete assignment of their 1H NMR spectra.
[3-D]2-硝基乙酰苯和[醇-18O]-1-(2-硝基苯基)乙醇被制备并用于合成带有标记的P3-L-(2-硝基苯基)乙酯的ATP(“笼型ATP”),其中同位素以氘的形式存在于硝基取代环的3-位上,或以18氧的形式存在于末端磷酸与硝基苯乙基团之间的桥接位置。氘代化合物的可用性使得其1H NMR光谱得以完全指认。