کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1313605 | 1499329 | 2015 | 4 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Selective trifluoromethylthiolation of heteroaromatic sp2 C–H bonds with the 2nd generation of trifluoromethanesulfenamide reagent Selective trifluoromethylthiolation of heteroaromatic sp2 C–H bonds with the 2nd generation of trifluoromethanesulfenamide reagent](/preview/png/1313605.png)
• Heterocycles are important in bioactive compounds.
• Very lipophilic SCF3 group increases the biodisponibility.
• Selective trifluoromethylthiolation with 2nd generation trifluoromethanesulfenamide.
• Easy access to functionalized CF3S-heterocycles.
By applying a well-established protocol of selective deprotonation of heteroarenes, the selective trifluoromethylthiolation of various heteroaromatic compounds has been performed, by using the 2nd generation of trifluoromethanesulfenamide reagent. With such strategy, functionalized heteroarenes could be synthesized as potential trifluoromethylthiolated building-blocks.
The 2nd generation of trifluoromethanesulfenamide reagent allows the selective trifluoromethylthiolation of heteroarenes via a selective deprotonation strategy.Figure optionsDownload as PowerPoint slide
Journal: Journal of Fluorine Chemistry - Volume 171, March 2015, Pages 78–81