Lithium hydro-(1-butyl)-bis-isopinocampheylborate: A reagent for asymmetric reduction of imines
- 31 December 1967
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 8 (22) , 2101-2103
- https://doi.org/10.1016/s0040-4039(00)91022-0
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Optical rotatory dispersion and absolute configuration—IIITetrahedron, 1965
- Hydroboration. XIX. The Reaction of Dissopinocampheylborane with Representative trans andHindered Olefins. Triisopinocampheyldiborane as a Reagent for the Configurational Assignment of Alcohols and Olefins via HydroborationJournal of the American Chemical Society, 1964
- Hydroboration. XVIII. The Reaction of Diisopinocampheylborane with Representative cis-Acyclic, Cyclic, and Bicyclic Olefins. A Convenient Systhesis of Optically Active Alcohols and Olefins of High Optical Purity and Established ConfigurationJournal of the American Chemical Society, 1964
- STEREOCHEMICAL CONSEQUENCES OF KETONE REDUCTIONS BY DIBORANE AND SUBSTITUTED BORANESJournal of the American Chemical Society, 1961