Fluorination With Aminosulfuranes
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Fluorination With Aminosulfuranes
Fluorination with aminosulfuranes is a chemical reaction that transforms oxidized organic compounds into organofluorine compounds. Aminosulfuranes selectively exchange hydroxyl groups for fluorine, but are also capable of converting carbonyl groups, halides, silyl ethers, and other functionality into organofluorides. Introduction Prior to the introduction of diethylaminosulfur trifluoride (DAST) in 1970 for the replacement of hydroxyl groups with fluoride, sulfur tetrafluoride was the reagent most commonly used to accomplish this transformation. However, sulfur tetrafluoride only reacts with the most acidic hydroxyl groups (its substrate scope is limited), and is difficult to handle, toxic, and capable of generating hydrogen fluoride upon hydrolysis. Thus, aminosulfurane reagents such as diethylaminosulfur trifluoride have largely replaced SF4 as the reagents of choice for replacement of hydroxyl groups with fluoride.von Halasz, P.; Glemser, O. ''Chem. Ber.'' 1970, ''103'', 594. Ami ...
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Organofluorine Compound
Organofluorine chemistry describes the chemistry of the organofluorines, organic compounds that contain the carbon–fluorine bond. Organofluorine compounds find diverse applications ranging from oil and water repellents to pharmaceuticals, refrigerants, and reagents in catalysis. In addition to these applications, some organofluorine compounds are pollutants because of their contributions to ozone depletion, global warming, bioaccumulation, and toxicity. The area of organofluorine chemistry often requires special techniques associated with the handling of fluorinating agents. The carbon–fluorine bond Fluorine has several distinctive differences from all other substituents encountered in organic molecules. As a result, the physical and chemical properties of organofluorines can be distinctive in comparison to other organohalogens. # The carbon–fluorine bond is one of the strongest in organic chemistry (an average bond energy around 480 kJ/molKirsch, Peer ''Modern fluoroorga ...
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