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Manganese benzylic lithium reagents

Ketones. Organomanganese reagents are formed by reaction of various halides (e.g., benzyl, aryl, heteroaryP) with Rieke Mn, which is prepared by reduction of manganese(II) halides with lithium naphthalenide in THF. Such reagents react with acid chlorides to afford ketones. [Pg.233]

CYCLOHEXYLIDENEACETALDEHYDES Manganese dioxide. CYCLOPENTANONES Magnesium. 1-Phenylthiocyclopropyltriphenylphosphonium fluoroborate. Simmons Smith reagent. Sodium tetracarbonylferrate(-II). CYCLOPENTENONES 3-Benzyl-5-(2-hydroxyethyl)-4-methyl-l,3-thiazolium chloride. Boron trifluoride etherate. Lithium dimethoxyphosphinylmethylide. Silver tetra-fluoroborate. Titanium tetrachloride. Triethyl phosphite. Vinyl triphenylphos-phonium bromide. [Pg.786]

See other pages where Manganese benzylic lithium reagents is mentioned: [Pg.2521]    [Pg.2520]    [Pg.1118]    [Pg.155]    [Pg.355]    [Pg.355]    [Pg.181]    [Pg.202]    [Pg.79]   
See also in sourсe #XX -- [ Pg.306 ]



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Benzyl-lithium

Lithium Reagents

Manganese reagents

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