Lithium diisobutylmethylaluminum hydride

Lithium diisobutylmethylaluminum hydride [1, 611, before Lithium dimethylamino-suifonylmethide]. Mol. wt. 164.19. [Pg.128]

Reducing agents Aluminum hydride. Bis-3-methyl-2-butylborane. n-Butyllithium-Pyridine. Calcium borohydride. Chloroiridic acid. Chromous acetate. Chromous chloride. Chromous sulfate. Copper chromite. Diborane. Diborane-Boron trifluoride. Diborane-Sodium borohydride. Diethyl phosphonate. Diimide. Diisobutylaluminum hydride. Dimethyl sulfide. Hexamethylphosphorous triamide. Iridium tetrachloride. Lead. Lithium alkyla-mines. Lithium aluminum hydride. Lithium aluminum hydride-Aluminum chloride. Lithium-Ammonia. Lithium diisobutylmethylaluminum hydride. Lithium-Diphenyl. Lithium ethylenediamine. Lithium-Hexamethylphosphoric triamide. Lithium hydride. Lithium triethoxyaluminum hydride. Lithium tri-/-butoxyaluminum hydride. Nickel-aluminum alloy. Pyridine-n-Butyllithium. Sodium amalgam. Sodium-Ammonia. Sodium borohydride. Sodium borohydride-BFs, see DDQ. Sodium dihydrobis-(2-methoxyethoxy) aluminate. Sodium hydrosulflte. Sodium telluride. Stannous chloride. Tin-HBr. Tri-n-butyltin hydride. Trimethyl phosphite, see Dinitrogen tetroxide. [Pg.516]

Lithium dicyclohexylamide, 321 Lithium diethylamide, 440 Lithium diisobutylmethylaluminum hydride, 292... [Pg.301]

A useful complement to the reactions above is based on the observation that the addition of lithium diisobutylmethylaluminum hydride (formed in situ from methyl-lithium and diisobutylaluminum hydride) to alkynes is a stereospecific trans addi-... [Pg.120]