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Sodium benzeneselenoate

The formation of aryl selenides from aryl halides and sodium benzeneselenoate occurs in the presence of nickel catalysts (Equation (41)).132 The trend in catalytic activity was shown to be... [Pg.385]

Silver(I) acetate, 396 Silver hexafluoroantimonate, 467 Silver imidazolate, 467 Silver nitrite-Mercury(II) chloride, 467-468 Silver(l) oxide, 468-469 Silver(II) oxide, 469 Silver perchlorate, 469-470 Silver tetrafluoroborate, 471 Silver(I) trifluoracetate, 471 Simmons-Smith reagent, 210-211, 472, 598 Sinularene, 246 Slaframine, 114, 115 Sodium amalgam, 473-475 Sodium-Ammonia, 472 Sodium benzeneselenoate, 475 Sodium bicarbonate, 476 Sodium bis(methoxyethoxy)aluminum hydride, 93, 476-477 Sodium borate, 322 Sodium borohydride, 477-479, 499 Sodium borohydride-Cobalt(IF) chloride, 479 Sodium borohydride-Methanesulfonic acid,... [Pg.338]

Sodium amalgam, 183, 326 Sodium-Ammonia, 355-356 Sodium benzeneselenoate, 356 Sodium bis(2-methoxyethoxy)aluminum hydride, 357,448 Sodium borohydride, 357-359 Sodium borohydride-Cadmium chloride, 359... [Pg.266]

Little C—Se bond formation by palladium catalysis has been reported, although these reactions should be feasible considering the ability of palladium complexes to catalyze C—S, C—P, and C—As bond formation. However, nickel complexes have been used for carbon-selenium bond formation. In 1985, Cristau and co-workers used bis(bipyridyl)nickel(ll) bromide to form aryl selenides from aryl halides and sodium benzeneselenoate. ... [Pg.1105]

See other pages where Sodium benzeneselenoate is mentioned: [Pg.580]    [Pg.439]    [Pg.439]    [Pg.439]    [Pg.587]    [Pg.182]    [Pg.237]    [Pg.580]    [Pg.439]    [Pg.439]    [Pg.439]    [Pg.587]    [Pg.182]    [Pg.237]   
See also in sourсe #XX -- [ Pg.356 ]

See also in sourсe #XX -- [ Pg.439 , Pg.440 ]

See also in sourсe #XX -- [ Pg.439 ]



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