Remarkably effective and simple syntheses of enantiomerically pure secondary carbinols from achiral ketones
- 18 November 1991
- journal article
- Published by Elsevier BV in Tetrahedron Letters
- Vol. 32 (47), 6835-6838
- https://doi.org/10.1016/0040-4039(91)80419-7
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- New enantioselective routes to biologically interesting compoundsPublished by Walter de Gruyter GmbH ,1990
- A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acidsTetrahedron Letters, 1990
- An efficient and catalytically enantioselective route to (S)-(-)-phenyloxiraneThe Journal of Organic Chemistry, 1988
- A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep synthesesJournal of the American Chemical Society, 1987
- Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implicationsJournal of the American Chemical Society, 1987
- Tritylketone und Tritylenone. Beiträge zur sterisch erzwungenen Michael‐Addition und zur diastereoselektiven Aldol‐AdditionHelvetica Chimica Acta, 1985
- Asymmetric reduction of trifluoromethyl ketones by actively fermenting yeastJournal of the Chemical Society, Chemical Communications, 1978