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- W3035147124 endingPage "14644" @default.
- W3035147124 startingPage "14635" @default.
- W3035147124 abstract "An efficient method for the synthesis of 2-(o-monofluoroalkenylaryl)quinazolinone derivatives was developed. In this context, the quinazolinone ring served as the inherent directing group, 2,2-difluorovinyl tosylate was used as the monofluoroolefin synthon, and Rh(III)-catalyzed C–H bond difluorovinylation of 2-arylquinazolinons was performed to give the corresponding monofluoroalkene-containing quinazolinons in yields of 65–92%. The method is characterized by broad synthetic utility, mild conditions, and high efficiency." @default.
- W3035147124 created "2020-06-19" @default.
- W3035147124 creator A5033080337 @default.
- W3035147124 creator A5043839950 @default.
- W3035147124 creator A5049321561 @default.
- W3035147124 creator A5058787076 @default.
- W3035147124 creator A5059049464 @default.
- W3035147124 date "2020-06-15" @default.
- W3035147124 modified "2023-10-12" @default.
- W3035147124 title "Rhodium-Catalyzed Merging of 2-Arylquinazolinone and 2,2-Difluorovinyl Tosylate: Diverse Synthesis of Monofluoroolefin Quinazolinone Derivatives" @default.
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