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Iodonium nitrate

The work of Lown and coworkers122 on iodonium nitrates has been reviewed.1 Addition of these reagents proceeds in a trans stereospecific manner, but with mediocre regiospecificity. The Lown group has also studied BrNC>3 and found it to be a more regiospecific reagent.123... [Pg.350]

Pyridine silver nitrateliodine monochloride Addition of iodonium nitrate to carbon-carbon double bonds... [Pg.142]

Diner UE, Lown JW (1971) Addition of iodonium nitrate to unsaturated hydrocarbons. Can J... [Pg.74]

Effects of the flavoprotein inhibitor, diphenylene iodonium sulfate, on ex vivo organic nitrate tolerance in the rat. J. Pharmacol. Exp. Ther. 293 (2000), p. 569-577... [Pg.52]

Iodine-copper(II) acetate, 267 Iodine-mercury(II) oxide, 267-268 Iodine monochloride, 268-269 Iodine-silver carboxylates, 268 Iodine-silver nitrate, 268 lodoamination, 265-266 Iodocarbamation, 264-265 Iodocarbonates, 263 2 Iodoestradiol, 267 2-Iodoestrone, 267 Iodoiactonization, 263-264 C,-Iodomethylcephalosporins, 273 Iodonium di-svm-collidine perchlorate, 269 19-Iodononadecanic acid, 488 Iodophenylbis(triphenylphosphine)palladium, 269... [Pg.335]

GLYCOSIDES Bromotrimethylsilane-Cobalt(II) bromide. Iodonium di-sym-collidine perchlorate. Mercury(II) nitrate. Silver imidazolate. Stannous chloride-Silver perchlorate. [Pg.241]

Significant amounts of the bicyclo[3.3.1]nonane adduct and of the octahydropental-enes were isolated also from the reaction of 3 with preformed iodine acetate and iodine acetate thallium (equation VS) whereas only the monocyclic 1,2-adducts were obtained from treatment of 3 with iodine azide, iodine isocyanate or iodine nitrate . The different propensity to give transannular products with these latter reagents has been related to the different positive charge density on carbons in the corresponding iodonium ion intermediates. [Pg.591]

Pummerer-like cyclization reactions were utilized to prepare spirocyclic oxindole derivatives <04OL1869, 04OL2849>. For example, treatment of 2-sulfenylindole 215 with an iodonium reagent in the presence of 2,6-lutidine produced thioimidate 216. Oxidation of the latter with cerium ammonium nitrate (CAN) gave spirooxindole 217. [Pg.133]

Single-crystal X-ray structures have been reported for the following aryl- and heteroaryliodo-nium salts diphenyliodonium triiodide [412], (2-methylphenyl)(2-methoxyphenyl)iodonium chloride [413], (2-methoxy-5-methylphenyl)(4-methoxy-2-methylphenyl)iodonium trifluoroacetate [414], (2-methoxy-5-methylphenyl)(4-methoxyphenyl)iodonium trifluoroacetate [415], a complex of diphenyliodonium tetrafluoroborate with pyridine [416], a complex of diphenyliodonium tetrafluoroborate with 1,10-phenanthroline [417], a complex of diphenyliodonium tetrafluoroborate with 18-crown-6 [418], 1-naphthylphenyliodonium tetrafluoroborate [419], 3,10-dimethyl-10//-dibenzo[, e]iodinium tetrafluoroborate [420], aryl(pentafluorophenyl)iodonium tetrafluoroborates [421], 4,4 -[bis(phenyliodonium)]-diphenylmethane ditriflate [422], [bis(4-methoxyphenyl)](diethylaminocarbodithioato)iodine(in) [423], di(p-tolyl)iodonium bromide [424], diphenyliodonium chloride, bromide and iodide [425,426], diphenyliodonium nitrate [427], diphenyliodonium tetrafluoroborate [428], thienyl(phenyl)iodonium salts [401], (anft-dimethanoanthracenyl)phenyliodonium tosylate and hexafluorophosphate [429] and 3-mesityl-5-phenylisoxazol-4-yl(phenyl)iodonium p-toluenesulfonate [409]. [Pg.82]


See other pages where Iodonium nitrate is mentioned: [Pg.678]    [Pg.678]    [Pg.254]    [Pg.238]    [Pg.678]    [Pg.678]    [Pg.254]    [Pg.238]    [Pg.945]    [Pg.974]    [Pg.369]    [Pg.43]    [Pg.108]    [Pg.345]    [Pg.957]    [Pg.945]    [Pg.85]    [Pg.137]    [Pg.957]    [Pg.39]    [Pg.945]    [Pg.108]    [Pg.345]    [Pg.361]    [Pg.253]    [Pg.302]    [Pg.381]    [Pg.279]    [Pg.176]    [Pg.68]    [Pg.40]   


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Iodonium

Iodonium nitrate double bonds

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