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Magnesium chloride sodium cyanoborohydride

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 Magnesium chloride sodium cyanoborohydride is mentioned: [Pg.210]    [Pg.470]    [Pg.239]    [Pg.631]    [Pg.361]    [Pg.783]    [Pg.729]    [Pg.8]    [Pg.1246]    [Pg.373]   


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Magnesium chloride

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Sodium cyanoborohydride

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