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Lithium tris borohydride cyclohexanones

The highest stereoselectivity reported to date apparently is that of lithium tris(5-butyl)borohydride. This reagent is sufficiently bulky that even 4-alkyl-cyclohexanones are reduced by equatorial approach, giving the axial alcohol. [Pg.137]

See other pages where Lithium tris borohydride cyclohexanones is mentioned: [Pg.911] [Pg.731] [Pg.14]

See also in sourсe #XX -- [ Pg.14 ]

See also in sourсe #XX -- [ Pg.8 , Pg.14 ]

See also in sourсe #XX -- [ Pg.8 , Pg.14 ]

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Lithium borohydride

Lithium tri

Lithium tris- borohydride