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- W4248560888 endingPage "16405" @default.
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- W4248560888 abstract "Abstract Described herein is an organocatalytic enantioselective desymmetrizing cycloisomerization of arylsulfonyl‐protected ynamide cyclohexanones, representing the first metal‐free asymmetric Conia‐ene‐type carbocyclization. This method allows the highly efficient and atom‐economical construction of a range of valuable morphans with wide substrate scope and excellent enantioselectivity (up to 97 % ee ). In addition, such a cycloisomerization of alkylsulfonyl‐protected ynamide cyclohexanones can lead to the divergent synthesis of normorphans as the main products with high enantioselectivity (up to 90 % ee ). Moreover, theoretical calculations are employed to elucidate the origins of regioselectivity and enantioselectivity." @default.
- W4248560888 created "2022-05-12" @default.
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- W4248560888 creator A5040262562 @default.
- W4248560888 creator A5056791108 @default.
- W4248560888 date "2019-09-18" @default.
- W4248560888 modified "2023-10-12" @default.
- W4248560888 title "Organocatalytic Enantioselective Conia‐Ene‐Type Carbocyclization of Ynamide Cyclohexanones: Regiodivergent Synthesis of Morphans and Normorphans" @default.
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