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Organocatalytic asymmetric conjugate addition of 2-fluoro-1,3-diketones to nitroalkenes

Authors
Kim, YubinKim, Yeon JooJeong, Hye ImKim, Dae Young
Issue Date
Sep-2017
Publisher
Elsevier BV
Keywords
Organocatalysts; Asymmetric catalysis; Conjugate addition; 2-Fluoro-1,3-diketones
Citation
Journal of Fluorine Chemistry, v.201, pp 43 - 48
Pages
6
Journal Title
Journal of Fluorine Chemistry
Volume
201
Start Page
43
End Page
48
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/7254
DOI
10.1016/j.jfluchem.2017.08.005
ISSN
0022-1139
1873-3328
Abstract
The organocatalytic enantioselective conjugate reaction of 2-fluoro-1,3-diketones to nitroalkenes promoted by chiral binaphthyl-modified squaramide has been achieved. Treatment of 2-fluoro-1,3-diketones with nitroalkenes under mild reaction conditions afforded the corresponding Michael products containing fluorinated quaternary carbon stereocenter with excellent enantioselectivity (up to 98% ee).
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