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- W4236692628 endingPage "1333" @default.
- W4236692628 startingPage "1329" @default.
- W4236692628 abstract "Abstract An unprecendented chiral sulfide catalyzed desymmetrizing enantioselective chlorination is disclosed. Various aryl‐tethered diolefins and diaryl‐tethered olefins afforded teralins and tricyclic hexahydrophenalene derivatives, respectively, bearing multiple stereogenic centers in high yields with excellent enantio‐ and diastereoselectivities. In contrast, the tertiary amine catalyst (DHQD) 2 PHAL led to a diastereomeric product. The products could be transformed into a variety of compounds, such as spiro‐N‐heterocycles." @default.
- W4236692628 created "2022-05-12" @default.
- W4236692628 creator A5007806208 @default.
- W4236692628 creator A5017613517 @default.
- W4236692628 creator A5075794924 @default.
- W4236692628 date "2019-01-09" @default.
- W4236692628 modified "2023-09-25" @default.
- W4236692628 title "Chiral Sulfide Catalysis for Desymmetrizing Enantioselective Chlorination" @default.
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- W4236692628 doi "https://doi.org/10.1002/ange.201811621" @default.
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