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Lead tetraacetate-Diphenyl disulfide

Iron(III) acetylacetonate, 211 Iron carbonyl, 152 Potassium ferricyanide, 255 Tri-jji-carbonylhexacarbonyldiiron, 320 Lead Compounds Iodine-Lead tetraacetate, 243 Lead tetraacetate, 62, 95, 155, 295 Lead tetraacetate-Diphenyl disulfide, 156... [Pg.409]

Lactonization, 93, 100, 370, 385-386, 413, 423,441,478-479,512 Lasiodiplodin, 386 Lead carbonate, 265 Lead tetraacetate, 199, 265-269 Lead tetrakistrifluoroacetate, 142, 143 Lead(lV) trifluoroacetate-Diphenyl disulfide, 269-270... [Pg.298]

OL-Hydroxysulfenylation. Lead tetraacetate and trifluoroacetic acid form lead(IV) trifluoroacetate in situ When an olefin and diphenyl disulfide are added to this reagent at 0 or -40°, a 3-trifluoroacetoxy sulfide is formed, which on basic work-up generates a thiohydrin (equation I). The reaction involves trans-addition. [Pg.441]

Oxidation, of diphenyl disulfide to methyl benzenesulfinate with lead tetraacetate in methanol, 46,62... [Pg.72]

Oxidative ring cleavage. Trost and Hiroi have developed a method for cleavage of cycloalkanones that involves essentially two steps selective sulfenyla-tion with diphenyl disulfide (5, 276-277 this volume) and oxidation with lead tetraacetate. The method is illustrated for estrone methyl ether as the substrate. Thus this five-membered ring ketone can be converted in high overall yield into... [Pg.313]

See other pages where Lead tetraacetate-Diphenyl disulfide is mentioned: [Pg.156]    [Pg.156]    [Pg.353]    [Pg.353]    [Pg.354]    [Pg.373]    [Pg.156]    [Pg.156]    [Pg.156]    [Pg.156]    [Pg.353]    [Pg.353]    [Pg.354]    [Pg.373]    [Pg.156]    [Pg.156]    [Pg.134]    [Pg.62]    [Pg.68]    [Pg.1013]    [Pg.32]   
See also in sourсe #XX -- [ Pg.156 ]

See also in sourсe #XX -- [ Pg.156 ]



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Diphenyl disulfide

Disulfides, diphenyl

Lead tetraacetate

Tetraacetate

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