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Optical magnesium hydride

Transformation of ketones to alcohols has been accomplished by many hydrides and complex hydrides by lithium aluminum hydride [55], by magnesium aluminum hydride [89], by lithium tris tert-butoxy)aluminum hydride [575], by dichloroalane prepared from lithium aluminum hydride and aluminum chloride [816], by lithium borohydride [750], by lithium triethylboro-hydride [100], by sodium borohydride [751,817], by sodium trimethoxyborohy-dride [99], by tetrabutylammonium borohydride [771] and cyanoborohydride [757], by chiral diisopinocampheylborane (yields 72-78%, optical purity 13-37%) [575], by dibutyl- and diphenylstannane [114], tributylstanrume [756] and others Procedure 21, p. 209). [Pg.107]

See other pages where Optical magnesium hydride is mentioned: [Pg.82]    [Pg.361]    [Pg.159]    [Pg.240]    [Pg.2]    [Pg.142]    [Pg.7]    [Pg.131]    [Pg.146]    [Pg.151]    [Pg.290]    [Pg.157]    [Pg.111]    [Pg.657]    [Pg.649]    [Pg.111]    [Pg.239]    [Pg.276]    [Pg.295]    [Pg.297]    [Pg.326]    [Pg.702]    [Pg.156]    [Pg.211]    [Pg.143]    [Pg.731]    [Pg.708]    [Pg.695]    [Pg.263]    [Pg.90]    [Pg.243]    [Pg.150]    [Pg.729]    [Pg.139]   
See also in sourсe #XX -- [ Pg.295 ]



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Magnesium hydride

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