Matches in SemOpenAlex for { <https://semopenalex.org/work/W2330280161> ?p ?o ?g. }
- W2330280161 endingPage "5850" @default.
- W2330280161 startingPage "5846" @default.
- W2330280161 abstract "Enantioselective trifluoromethylthiolation, especially of alkenes, is a challenging task. In this work, we have developed an efficient approach for enantioselective trifluoromethylthiolating lactonization by designing an indane-based bifunctional chiral sulfide catalyst and a shelf-stable electrophilic SCF3 reagent. The desired products were formed with diastereoselectivities of >99:1 and good to excellent enantioselectivities. The transformation represents the first enantioselective trifluoromethylthiolation of alkenes and the first enantioselective trifluoromethylthiolation that is enabled by a catalyst with a Lewis basic sulfur center." @default.
- W2330280161 created "2016-06-24" @default.
- W2330280161 creator A5007806208 @default.
- W2330280161 creator A5063329658 @default.
- W2330280161 creator A5069365973 @default.
- W2330280161 creator A5075794924 @default.
- W2330280161 creator A5081174928 @default.
- W2330280161 date "2016-03-30" @default.
- W2330280161 modified "2023-09-24" @default.
- W2330280161 title "Enantioselective Trifluoromethylthiolating Lactonization Catalyzed by an Indane-Based Chiral Sulfide" @default.
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