Despite the undisputed importance of organofluorine compounds, for example, in biomedical applications, the generation of fluorinated carbon stereocenters by CΓF bond-forming reactions remains rare and particularly challenging. [1, 2] Recently, the first catalytic, enantioselective fluorination of b
β¦ LIBER β¦
The Mechanism of Catalytic Enantioselective Fluorination: Computational and Experimental Studies
β Scribed by Stefano Piana; Ingrid Devillers; Antonio Togni; Ursula Rothlisberger
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 129 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0044-8249
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