Silver(I) Oxide Catalyzed C/S–H Trifluoromethylation of Arenes and Heteroarenes with Sodium Trifluoromethanesulfinate

Abstract We present a general and scalable approach for the C(sp2)–H or S–H trifluoromethylation of arenes and heteroarenes. This method employs bench-stable CF3SO2Na as the CF3 source, with Ag2O serving as the catalyst and K2S2O8 as the oxidant. Notably, the protocol features broad functional-group compatibility, mild conditions, and high regioselectivity. Furthermore, it is applicable to biologically relevant molecules such as caffeine, pentoxifylline, ganciclovir triacetate, and mercaptopurine.

Authors

Publication Details

Journal
Synlett
Published
2025-05-09
DOI
https://doi.org/10.1055/s-0043-1775481
Citations
2
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
1.58
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article

Silver(I) Oxide Catalyzed C/S–H Trifluoromethylation of Arenes and Heteroarenes with Sodium Trifluoromethanesulfinate

Kishore Natte, Sandeep Kumawat, Km Sadhana, K. Jyothi
2 citations
Synlett
Fluorine in Organic Chemistry
1.58
article

Silver(I) Oxide Catalyzed C/S–H Trifluoromethylation of Arenes and Heteroarenes with Sodium Trifluoromethanesulfinate

Kishore Natte, Sandeep Kumawat, Km Sadhana, K. Jyothi
article en
2 citations

Abstract

Abstract We present a general and scalable approach for the C(sp2)–H or S–H trifluoromethylation of arenes and heteroarenes. This method employs bench-stable CF3SO2Na as the CF3 source, with Ag2O serving as the catalyst and K2S2O8 as the oxidant. Notably, the protocol features broad functional-group compatibility, mild conditions, and high regioselectivity. Furthermore, it is applicable to biologically relevant molecules such as caffeine, pentoxifylline, ganciclovir triacetate, and mercaptopurine.

SynlettVol. 36(15)
Openalex Percentile: Top 17%
Fluorine in Organic Chemistry
1.58
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