![Enantioselective reduction of ketones with NaBH4/diglyme possibly catalysed by trialkyl borate: optically active sec-alcohols from prochiral ketones with catalytic (−)-menthol: autocatalysis option - ScienceDirect Enantioselective reduction of ketones with NaBH4/diglyme possibly catalysed by trialkyl borate: optically active sec-alcohols from prochiral ketones with catalytic (−)-menthol: autocatalysis option - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0957416604009498-gr1.jpg)
Enantioselective reduction of ketones with NaBH4/diglyme possibly catalysed by trialkyl borate: optically active sec-alcohols from prochiral ketones with catalytic (−)-menthol: autocatalysis option - ScienceDirect
![NaBH4, LiAlH4, DIBAL Reduction Mechanism, Carboxylic Acid, Acid Chloride, Ester, & Ketones - YouTube NaBH4, LiAlH4, DIBAL Reduction Mechanism, Carboxylic Acid, Acid Chloride, Ester, & Ketones - YouTube](https://i.ytimg.com/vi/Pp0LeL0SkRg/sddefault.jpg)
NaBH4, LiAlH4, DIBAL Reduction Mechanism, Carboxylic Acid, Acid Chloride, Ester, & Ketones - YouTube
![SOLVED:Introduction: The reduction of carbonyl compounds to alcohols using metal hydride reagents is common reaction_ Two of the most common metal hydride reducing agents are sodium borohydride (NaBH4) and lithium aluminum hydride ( SOLVED:Introduction: The reduction of carbonyl compounds to alcohols using metal hydride reagents is common reaction_ Two of the most common metal hydride reducing agents are sodium borohydride (NaBH4) and lithium aluminum hydride (](https://cdn.numerade.com/ask_images/5d23360fd4054ea0b61b3d4176f984a4.jpg)
SOLVED:Introduction: The reduction of carbonyl compounds to alcohols using metal hydride reagents is common reaction_ Two of the most common metal hydride reducing agents are sodium borohydride (NaBH4) and lithium aluminum hydride (
![Reduction of aldehydes ketones nitriles Lithium tetrahydridoaluminate(III) (lithium aluminium hydride) LiAlH4 or NaBH4 sodium tetrahydridoborate(III) (sodium tetraborohydride) to primary & secondary alcohols advanced A level organic chemistry revision ... Reduction of aldehydes ketones nitriles Lithium tetrahydridoaluminate(III) (lithium aluminium hydride) LiAlH4 or NaBH4 sodium tetrahydridoborate(III) (sodium tetraborohydride) to primary & secondary alcohols advanced A level organic chemistry revision ...](https://docbrown.info/page06/WMtestsNotes/mech83b.gif)