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Benzeneselenol, 2,4,6-tris

CdSe2C36HM), Benzeneselenol, 2,4,6-tris(l,l-dimethylethyl)-, cadmium salt, [137358-89-5], 31 22... [Pg.326]

Tris(phenylseieno)borane, B(SeCsH5)3. Mol. wt. 479.02, m.p. 152-153°, decomposes slowly in air. The borane is prepared in 84% yield by the reaction of benzeneselenol with boron tribromide at 25°. ... [Pg.562]

ALLYLIC ALCOHOLS Benzeneselenol. 9-Borabicyclo[3.3.11 nonane. n-Butyllithium. Cuprous iodide-Grignard reagents. Diethylaluminum 2,2,6,6-tetramethylpiperidide. Fluorodimethoxyborane. rrans-l-Tri-n-butylstannyl-propene-3-tetrahydropyranyl ether. [Pg.785]

Although benzeneselenol adds across the triple bond of phenylacetylene in the presence of molecular oxygen to give the corresponding vinyl selenide (equation 15), inactivated acetylenes proceed very slowly under similar conditions". However, the addition of PhSeH to inactivated acetylenes has been achieved in the presence of a catalytic amount of diselenide upon irradiation (equation 16)". Evidence that these reactions proceed via a radical mechanism is also given. Tris(phenylseleno)borane and tris(methylseleno)borane react also with terminal acetylenes to give (Z)-vinyl selenides". ... [Pg.925]

See other pages where Benzeneselenol, 2,4,6-tris is mentioned: [Pg.329]    [Pg.339]    [Pg.339]    [Pg.346]    [Pg.346]    [Pg.346]    [Pg.339]    [Pg.339]    [Pg.342]    [Pg.346]    [Pg.346]    [Pg.346]    [Pg.329]    [Pg.339]    [Pg.339]    [Pg.346]    [Pg.346]    [Pg.346]    [Pg.642]    [Pg.437]    [Pg.240]    [Pg.339]    [Pg.339]    [Pg.342]    [Pg.346]    [Pg.346]    [Pg.346]   


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Benzeneselenol

Benzeneselenol, 2,4,6-tris salt

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