Gary B. Fisher
University of California, Santa Cruz(US)
Publications by Year
Research Areas
Chemical Synthesis and Analysis, Coordination Chemistry and Organometallics, Asymmetric Hydrogenation and Catalysis, Asymmetric Synthesis and Catalysis, Organoboron and organosilicon chemistry
Most-Cited Works
- → Aminoborohydrides. 4. The Synthesis and Characterization of Lithium Aminoborohydrides: A New Class of Powerful, Selective, Air-Stable Reducing Agents(1994)94 cited
- → Lithium Aminoborohydrides 16. Synthesis and Reactions of Monomeric and Dimeric Aminoboranes(2008)65 cited
- → Boranes in Synthesis. 6. A New Synthesis of .beta.-Amino Alcohols from Epoxides. Use of Lithium Amides and Aminoborane Catalysts To Synthesize .beta.-Amino Alcohols from Terminal and Internal Epoxides in High Yield(1994)55 cited
- → Synthesis and characterization of lithium aminoborohydrides: A new class of powerful reducing agents(1992)52 cited
- → Aminoborohydrides. 8. A facile reduction of aliphatic and benzylic azides to the corresponding amines in high yield and purity using lithium N,N-dimethylaminoborohydride(1995)45 cited
- → Boranes in Synthesis. 5. The Hydroboration of Enamines with Mono- and Dialkylboranes. Asymmetric Synthesis of .beta.-Amino Alcohols of Moderate Enantiomeric Purity from Aldehyde Enamines(1995)37 cited
- → Aminoborohydrides. 3. A facile reduction of tertiary amides to the corresponding amines and alcohols in high purity using lithium aminoborohydrides. Sterically controlled selective CN or CO bond cleavage(1993)36 cited
- → Unusual directive effects in the hydroboration of .beta.,.beta.-disubstituted enamines. Conversion of .alpha.-substituted aldehydes to the corresponding alkenes and .beta.-amino alcohols(1991)34 cited
- → Aminoborohydrides. 9. Selective reductions of aldehydes, ketones, esters, and epoxides in the presence of a nitrile using Lithium N,N-dialkylaminoborohydrides(1997)27 cited
- → Boranes in synthesis. 2. Asymmetric synthesis of β-amino alcohols. A facile conversion of 2-amino acetophenones to the corresponding β-amino alcohols in high enantiomeric purity(1994)22 cited