Department of Chemistry, Taras Shevchenko National University of Kyiv , Volodymyrska 64, Kyiv 01601, Ukraine.
Org Lett. 2015 Jan 16;17(2):226-9. doi: 10.1021/ol503300m. Epub 2014 Dec 29.
Novel aliphatic (19)F-substituted amino acid was designed as a (19)F NMR label for peptide studies. The synthesis was performed in 11 steps and 9% overall yield from a commercially available starting material. The key transformation was a decarboxylative fluorination of an aliphatic carboxylic acid with XeF2 in C6F6.
新型脂肪族(19)F 取代氨基酸被设计为用于研究肽的(19)F NMR 标记物。该合成是从商业上可获得的起始原料出发,经 11 步反应以 9%的总收率完成的。关键转化是在六氟苯中用氙化氟(XeF2)对脂肪族羧酸进行脱羧氟化。