Catalytic asymmetric fluorinations.

Symplectic ID
33488
Source
PubMed
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Friday, 4 September, 2026 - 21:44
DOI
10.1039/b603163c
Publication Date
Wednesday, 7 June, 2006
First Page
2065
Last Page
2075
Keywords
Catalysis
Cinchona Alkaloids
Hydrocarbons, Fluorinated
Imidazolidines
Metals
Proline
Stereoisomerism
Authors
Bobbio, C
Gouverneur, V
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0
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Abstract
The appearance of structurally diverse fluorinating reagents displaying a large spectrum of reactivity has been critical to the development of the catalytic asymmetric fluorination processes known to date. In this article, we discuss how this area of research emerged and which strategies have allowed for the successful development of both nucleophilic and electrophilic catalytic enantioselective fluorinations. We also present the fundamental understanding of catalytic activity and enantioselectivity for the most efficient processes and highlight the first synthetic application with the preparation of a complex fluorinated target.
ISSN
1477-0520
Journal Title
Org Biomol Chem
Volume
4
Issue
11
ID at Source
16729117
Publication Status
Published
Open access
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chem0068