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- W2061058332 abstract "Abstract The asymmetric alkylation of 2-phenyl-1,3-dioxan-5-one was achieved via the RAMP-hydrazone. Regeneration of the ketone followed by setreoselective reduction and ozonolysis, gave the protected 2-deoxy-L-ribose, 3,5-O-benzyldiene-2-deoxy-L-erythro-pentoaldose with 98% e.e. Removal of the benzylidene yielded the unnatural 2-deoxy-L-ribose." @default.
- W2061058332 created "2016-06-24" @default.
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- W2061058332 date "2000-10-10" @default.
- W2061058332 modified "2023-09-23" @default.
- W2061058332 title "ChemInform Abstract: Synthesis of 3,5-O-Benzylidene-2-deoxy-L-riboaldose from 5,5-Dihydroxy-2-phenyl-1,3-dioxane." @default.
- W2061058332 cites W2950330108 @default.
- W2061058332 doi "https://doi.org/10.1002/chin.200041165" @default.
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