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- W4200009713 endingPage "605" @default.
- W4200009713 startingPage "595" @default.
- W4200009713 abstract "A new catalytic protocol for the synthesis of selenoesters from aryl iodides and diaryl diselenides has been developed, where formic acid was employed as an efficient, low-cost, and safe substitute for toxic and gaseous CO. This protocol presents a high functional group tolerance, providing access to a large family of selenoesters in high yields (up to 97%) while operating under mild reaction conditions, and avoids the use of selenol which is difficult to manipulate, easily oxidizes, and has a bad odor. Additionally, this method can be efficiently extended to the synthesis of thioesters with moderate-to-excellent yields, by employing for the first time diorganyl disulfides as precursors." @default.
- W4200009713 created "2021-12-31" @default.
- W4200009713 creator A5023086099 @default.
- W4200009713 creator A5041279745 @default.
- W4200009713 creator A5055579743 @default.
- W4200009713 creator A5062510141 @default.
- W4200009713 creator A5068465479 @default.
- W4200009713 creator A5074521040 @default.
- W4200009713 date "2021-12-28" @default.
- W4200009713 modified "2023-10-14" @default.
- W4200009713 title "Palladium-Catalyzed Carbonylative Synthesis of Aryl Selenoesters Using Formic Acid as an <i>Ex Situ</i> CO Source" @default.
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- W4200009713 doi "https://doi.org/10.1021/acs.joc.1c02608" @default.
- W4200009713 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34962405" @default.