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- W4306646799 abstract "Abstract Herein, we report a practical method for de novo preparation of imino‐ d ‐ribitol and C ‐azanucleosides. The diastereopure Imino‐ d ‐ribitol was synthesized on a multigram scale by simple manipulation, and late‐stage anomeric derivatization by regio‐ and diastereoselective electrochemical C(sp 3 )−H activation enabled the efficient synthesis of the corresponding C ‐azanucleosides with high β‐selectivity." @default.
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- W4306646799 date "2022-11-21" @default.
- W4306646799 modified "2023-10-16" @default.
- W4306646799 title "Stereoselective Production of Imino‐<scp>d</scp>‐ribitol and <i>C</i>‐Azanucleosides through Electrochemical C−H Functionalization" @default.
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- W4306646799 doi "https://doi.org/10.1002/ejoc.202201046" @default.
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