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- W4243161105 startingPage "7548" @default.
- W4243161105 abstract "Abstract A highly efficient synthesis of the enantioenriched tetrahydro‐β‐carbolines was developed by using a chiral phosphoric acid catalyzed Pictet–Spengler reaction of indolyl dihydropyridines. The reaction proceeds under mild reaction conditions to afford the desired chiral tetrahydro‐β‐carbolines in good to excellent yields (up to 96 %) and high enantioselectivities (up to 99 % ee ). With this method, a formal synthesis of tangutorine and a total synthesis of deplancheine were achieved in a highly efficient manner." @default.
- W4243161105 created "2022-05-12" @default.
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- W4243161105 date "2017-05-23" @default.
- W4243161105 modified "2023-10-16" @default.
- W4243161105 title "Construction of Chiral Tetrahydro-β-Carbolines: Asymmetric Pictet-Spengler Reaction of Indolyl Dihydropyridines" @default.
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- W4243161105 doi "https://doi.org/10.1002/ange.201703178" @default.
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