Titlebook: Hypervalent Iodine Chemistry; Modern Developments Thomas Wirth Book 2003 Springer-Verlag Berlin Heidelberg 2003 Biochemie.Biochemistry.Ino

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Weiterbildung Gynäkologie und Geburtshilfeesis. The most important recent methods involve the radical decarboxylative alkylation of organic substrates with [bis(acyloxy)iodo]arenes, spirocyclization of .- and .-substituted phenols, the intramolecular oxidative coupling of phenol ethers, and the reactions of iodonium salts and ylides. A sign

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Weiterbildung Gynäkologie und Geburtshilfef aryl-λ.-iodanes with organic substrates are considered first and are loosely organized by functional group, separate sections being devoted to carbon-azide and carbon-fluorine bond formation. Arylations and alkenylations of nucleophilic species with diaryliodonium and alkenyl(aryl)iodonium salts,

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https://doi.org/10.1007/978-3-662-49415-8es with heteroatom substrates derived from third-row elements and beyond are considered first, and an unusual example of heteroatom-heteroatom bond formation with diaryliodonium salts is then discussed. Finally, the use of sulfonylimino(aryl)iodanes for imidations of phosphorus, sulfur, selenium, an

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Welfare Aspects of Transgenic Animals) diacetate (PIDA) and phenyliodine(III) bis(trifluoroacetate) (PIFA) have received a great deal of attention due to low toxicity, ready availability, easy handling, and reactivities similar to that of heavy metal reagents and anodic oxidation. A variety of available reactions for natural product sy

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Reactivities, Properties and Structures,th external nucleophiles, is a facile low energy process. A very high leaving group ability of λ.-iodanyl groups is among the most important features of λ.-iodanes, which makes it possible to generates highly reactive species such as carbenes, nitrenes, cations, and arynes under mild conditions and

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C-C-Bond Forming Reactions,esis. The most important recent methods involve the radical decarboxylative alkylation of organic substrates with [bis(acyloxy)iodo]arenes, spirocyclization of .- and .-substituted phenols, the intramolecular oxidative coupling of phenol ethers, and the reactions of iodonium salts and ylides. A sign