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Recently, we reported the intermolecular transfer of the alkylidene groups of arylbromonium ylides to aryl halides (iodides, bromides, and chlorides) yielding a variety of aryliodonium, bromonium, and chloronium ylides under thermal or metal-catalyzed conditions. See: Ochiai, M.; Tada, N.; Okada, T.; Sota, A.; Miyamoto, K. J. Am. Chem. Soc. 2008, 130, 2118.
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Recently, we reported the intermolecular transfer of the alkylidene groups of arylbromonium ylides to aryl halides (iodides, bromides, and chlorides) yielding a variety of aryliodonium, bromonium, and chloronium ylides under thermal or metal-catalyzed conditions. See: Ochiai, M.; Tada, N.; Okada, T.; Sota, A.; Miyamoto, K. J. Am. Chem. Soc. 2008, 130, 2118.
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For transylidations between a diazo compound and a halonium ylide, see: a
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For instance, p-nitrophenyliodonium dinitromethylide is more stable to thermal decomposition than phenyliodonium dinitromethylide, but the reverse is true for the iodonium ylides derived from dimedone. See Ref 4d.
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For instance, p-nitrophenyliodonium dinitromethylide is more stable to thermal decomposition than phenyliodonium dinitromethylide, but the reverse is true for the iodonium ylides derived from dimedone. See Ref 4d.
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