Symplectic ID:
33488
Source:
PubMed
This is the preferred source?:
1
Last Synced with Symplectic:
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
Editors list has been truncated:
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:
Publication Date - Display month part?:
Publication Date - Display day part?:
SSO preference:
chem0068