Iodide synthesis

See also Aluminum(III) iodide, synthesis 39 Gallium(II) chloride, synthesis 37... 

Calcium dihydrogen orthophosphate 1-hydrate, synthesis 5 Calcium hydrogen orthophosphate, synthesis 6 Arsenic(III) fluoride, synthesis 50 Bismuth (III) iodide, synthesis 38 Vanadium(II) chloride, synthesis... 

Fujimura, M., Nakazawa, T and Murata, I., A novel coupling reaction of 1-azulylmethyl-trimcthylammonium iodide synthesis of l,2-bi.s(I-azulyl)ethane and 12.2.2.21(1.3)-azulenophane. Tetrahedron Lett., 825, 1979. 

Dondoni, A, Fantin, G, Fogagnolo, M, Merino, P, Regio- and stereoselective conjugate addition of nitrogen nucleophiles to 2-alkenyl iV-methylthiazolium iodides. Synthesis of 3-epi-daunosamine and some lincosamine analogues. Tetrahedron, 46, 6167-6184, 1990 see also Ref. [97b]. 

Ipodate, which inhibits the conversion of thyroxine to triiodothyronine, is useful in reducing the intensity of thyroid storm. Sympathoplegic drugs are also useful, and propranolol is the most commonly used agent. Further release of hormone from the gland is blocked by intravenous administration of sodium iodide supplemented by oral potassium iodide. Synthesis is inhibited by oral or, if necessary, parenteral antithyroid drugs. Corticosteroids are sometimes used. 

Barium iodate 1-hydrate, synthesis 4 Indium(I) bromide, synthesis 6 Hexachlorodisiloxane, synthesis 7 Trichlorosilanethiol, synthesis 8 Tris(acetylacetonato)silicon chloride, synthesis 9 Titanium(III)chloride, synthesis 11 Bis[tris(acetylacetonato)titanium(IV)] hexachloro-titanate(IV), synthesis 12 Zirconium(IV) iodide, synthesis 13 (Triphenyl) aminophosphonium chloride, synthesis 19 (Dimethylamido)phosphoryl dichloride, synthesis 20 Bis(dimethylamido)phosphoryl chloride, synthesis 21 Trimeric and tetrameric phosphonitrilic bromides, synthesis 23 Phosphorus(V) chloride-boron trichloride complex, synthesis 24... 

Methylbromoarsines, synthesis 26 Vanadium(III) fluoride, synthesis 27 Sulfur(IV) fluoride, synthesis 33 Peroxydisulfuryl difluoride, synthesis 34 Trichloro(tripyridine)chromium(III), synthesis 36 Tris(3-bromoacetylacetonato)chromium(III), synthesis 37 Trichloro(tripyridine)molybdenum(III), synthesis 39 Uranyl chloride 1-hydrate, synthesis 41 Rhenium(III) iodide, synthesis 50 Potassium hexachlororhenate(IV) and potassium hexa-bromorhenate(IV), synthesis 51 Iron-labeled cyclopentadienyl iron complexes, synthesis 54 Inner complexes of cobalt(III) with diethylenetriamine, synthesis 56... 

There have been further applications of MesSil and MesSiBr as dealkylating agents for ethers, esters, phosphonic acid esters, and alcohols, the last reaction using McsSil being a useful alkyl iodide synthesis. MesSil also converts acetals into ketones or sulphoxides into sulphides, whilst a mixture of PhSiMes and I2 is capable of dealkylating esters at ca. 110°C. ... 

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