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Reduction of aldehydes and ketones with tetraalkylammonium borohydrides
Authors:Douglas J. Raber  Wayne C. Guida  Douglas C. Shoenberger
Affiliation:Department of Chemistry, University of South Florida, Tampa, Florida 33620 U.S.A.;Department of Chemistry, Eckerd College, St. Petersburg, Florida 33733 U.S.A.
Abstract:Misinterpretations regarding the selectivity of tetraalkylaminonium borohydride reductions in dichloromethane are resolved. Tetrabutyl ammonium borohydride offers several advantages, but both it and tetraethyl ammoniumborohydride are highly useful synthetic reagents.
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