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Oximes trimethylsilyl chlorochromate

Potassium hydroxide, 258 Trimethylsilyl chlorochromate, 327 of carbon-carbon double bonds substituted by heteroatoms m-Chloroperbenzoic acid, 76 of oximes to carbonyl compounds Lithium aluminum hydride-Hexa-methylphosphoric triamide, 159 Titanium(III) chloride-Diisobutylalu-minum hydride, 303 Trimethylsilyl chlorochromate, 327 of protected alcohols Chlorodimethylthexylsilane, 74 Formic acid, 137 p-Methoxyphenol, 181 of thioacetals and -ketals Methoxy(phenylthio)trimethyl-silylmethane, 182... [Pg.366]

Oximes play an important role as protecting groups due to their hydrolytic stability. Their frequent use has provided incratives far the develqnnent of newo deoximation reagents such as pyridinium chlorochromate, Raney nickel, triethylammonium chlorochromate, pyridinium chlorochromate-H202, nitrogen tetroxide, trimethylsilyl chlorochromate, H2O2 over titanium silicalite-1, Dowex-SO, dimethyl dioxirane, zirconium sulfophenyl phosphonate, AT-haloamides, and bismuth dil( ide (22). [Pg.297]

See other pages where Oximes trimethylsilyl chlorochromate is mentioned: [Pg.285]    [Pg.285]    [Pg.369]    [Pg.83]   
See also in sourсe #XX -- [ Pg.285 ]

See also in sourсe #XX -- [ Pg.285 ]

See also in sourсe #XX -- [ Pg.7 , Pg.285 ]

See also in sourсe #XX -- [ Pg.7 , Pg.285 ]

See also in sourсe #XX -- [ Pg.285 ]



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Chlorochromate

Oximes trimethylsilylation

Trimethylsilyl chlorochromate

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