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Synthesis 2021; 53(09): 1597-1604
DOI: 10.1055/s-0040-1705976
DOI: 10.1055/s-0040-1705976
paper
An Efficient Substrate-Induced Method for the Synthesis of CF3-Substituted Cyclopropanes by Metal-Free Reaction of Trifluoromethyl Styrylisoxazoles with Nitromethane
We thank the Voluntary Program of China Academy of Chinese Medical Sciences (ZZ0908028) for financial support.
Abstract
A series of (trifluoromethyl)cyclopropanes (TFCPs) tolerating a broad range of functional groups, known as tert-butyl bioisosteres, have been obtained from the cyclization reaction between nitromethane and 5-[β-(trifluoromethyl)styryl]isoxazoles in 70–94% yields and 75:25 to 90:10 dr. This method offers practical access to this cyclopropyl moiety of pharmacological interest, employing an inorganic base under phase-transfer conditions.
Key words
styrylisoxazole - cyclization - trifluoromethyl - cyclopropane - inorganic base - phase-transfer catalystSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0040-1705976.
- Supporting Information
Publikationsverlauf
Eingereicht: 02. Oktober 2020
Angenommen nach Revision: 21. Oktober 2020
Artikel online veröffentlicht:
19. November 2020
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Georg Thieme Verlag KG
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