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- W2950579845 abstract "Abstract Intramolecular 1,3-dipolar cycloadditions of nitrones formed from 3-O-allyl- d -glucose and d -altrose (both with threo-configuration at C-2,3) afford oxepanes selectively whereas the same reactions of nitrones derived from 3-O-allyl- d -allose and d -mannose (both with erythro-configuration at C-2,3) give tetrahydropyrans selectively." @default.
- W2950579845 created "2019-06-27" @default.
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- W2950579845 date "2010-05-25" @default.
- W2950579845 modified "2023-09-23" @default.
- W2950579845 title "ChemInform Abstract: Ring-Selective Synthesis of O-Heterocycles from Acyclic 3-O-Allyl-monosaccharides via Intramolecular Nitrone-Alkene Cycloaddition." @default.
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- W2950579845 doi "https://doi.org/10.1002/chin.200127191" @default.
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