Enantioselective Formation of Stereogenic Carbon–Fluorine Centers by a Simple Catalytic Method
- 6 June 2005
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 117 (24) , 3769-3772
- https://doi.org/10.1002/ange.200500395
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- Direct Organocatalytic α-Fluorination of Aldehydes and KetonesSynlett, 2005
- Direct Proline-Catalyzed Asymmetric α-Aminoxylation of Aldehydes and KetonesThe Journal of Organic Chemistry, 2004
- Direct Proline‐Catalyzed Asymmetric α‐Aminoxylation of KetonesAngewandte Chemie, 2004
- Direct Catalytic Enantioselectiveα-Aminoxylation of Ketones: A Stereoselective Synthesis ofα-Hydroxy andα,α′-Dihydroxy KetonesAngewandte Chemie, 2004
- Enantioselective halogenation reactionsChemical Communications, 2004
- Fluorinated Carbonyl and Olefinic Compounds: Basic Character and Asymmetric Catalytic ReactionsChemical Reviews, 2003
- Dinitrogen Reduction by Tm(II), Dy(II), and Nd(II) with Simple Amide and Aryloxide LigandsJournal of the American Chemical Society, 2002
- Fluorine substituent effects (on bioactivity)Published by Elsevier ,2001
- Fluorine chemistry statistics: numbers of organofluorine compounds and publications associated with fluorine chemistryJournal of Fluorine Chemistry, 1999
- Nonracemic α-Fluoro Aldehydes: Asymmetric Synthesis of 4-Deoxy-4-fluoro-d-arabinopyranoseThe Journal of Organic Chemistry, 1997