Organocatalytic asymmetric synthesis of 3-difluoroalkyl 3-hydroxyoxindoles
2012
Liu, Yun-Lin | Zhou, Jian
We report the first example of highly enantioselective organocatalytic synthesis of 3-difluoroalkyl substituted 3-hydroxyoxindoles. The total synthesis of the difluoro analogue of convolutamydine E was achieved by this method.
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Bibliographic information
Publisher
The Royal Society of Chemistry
Other Subjects
Enantioselectivity; Stereoselective synthesis
Language
English
Type
Journal Article; Text
2024-02-28
MODS
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