Selective reductions. 53. Asymmetric reduction of α-fluoromethyl ketones with B-chlorodiisopinocampheylborane and B-isopinocampheyl-9-borabicyclo[3.3.1]nonane. Combined electronic and steric contributions to the enantiocontrol process
- 30 June 1994
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 5 (6) , 1075-1086
- https://doi.org/10.1016/0957-4166(94)80057-x
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- A microbially-based approach for the synthesis of chiral secondary alcohols bearing the difluoromethyl or chlorodifluoromethyl groupJournal of Fluorine Chemistry, 1992
- Asymmetric reduction with chiral organoboranes based on .alpha.-pineneAccounts of Chemical Research, 1992
- The boron approach to asymmetric synthesisPure and Applied Chemistry, 1991
- Synthesis of optically active fluorinated materials by use of immobilized enzymes for asymmetric hydrolysisJournal of Fluorine Chemistry, 1988
- Selective reductions. 40. A critical examination of the relative effectiveness of various reducing agents for the asymmetric reduction of different classes of ketonesThe Journal of Organic Chemistry, 1987
- The synthesis of optically active building blocks carrying a monofluoromethyl groupJournal of Fluorine Chemistry, 1987
- Selective reductions. 37. Asymmetric reduction of prochiral ketones with B-(3-pinanyl)-9-borabicyclo[3.3.1]nonaneThe Journal of Organic Chemistry, 1985
- Kinetics of reductions of substituted benzaldehydes with B-alkyl-9-borabicyclo[3.3.1]nonane (9-BBN)Journal of the American Chemical Society, 1982
- Proton-transfer reactions. II. Effects of internal return on reactivity difference between alkoxide-promoted eliminations in tert-butyl alcohol and ethyl alcoholJournal of the American Chemical Society, 1981
- A New Synthesis of Ketones Containing One Perfluoroalkyl Group1,2Journal of the American Chemical Society, 1956