化学
亲核细胞
产量(工程)
硫黄
放射化学
分子
药物化学
组合化学
催化作用
有机化学
冶金
材料科学
作者
Min Ho Jeon,Young‐Do Kwon,Min Pyeong Kim,Gianluca Bartolini Torres,Jeong Kon Seo,Jeongmin Son,Young Hoon Ryu,Sung You Hong,Joong‐Hyun Chun
出处
期刊:Organic Letters
[American Chemical Society]
日期:2021-03-16
卷期号:23 (7): 2766-2771
被引量:23
标识
DOI:10.1021/acs.orglett.1c00671
摘要
Synthesis of sulfamoyl [18F]fluorides has been a challenging topic owing to the inefficient nucleophilic radiofluorination of sulfamoyl derivatives. Herein, we report an 18F/19F isotopic exchange approach to synthesize various sulfamoyl [18F]fluorides, otherwise inaccessible via direct synthesis from amines, with high radiochemical yields up to 97% (30 examples). This late-stage labeling protocol offers an efficient route to yield functionalized molecules by diversifying the chemical library possessing sulfamoyl functionalities through nucleophilic 18F incorporation within nitrogen-containing sulfur(VI) frameworks.
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