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- W2062824249 abstract "A key intermediate 15 was prepared via successive glycosidations of 1,6-anhydro maltose derivative 8 with glycosyl donors 6 and then with 11, cyclized under a diluted condition, and deprotected to give the title compound. Every glycosidation, including the cyclization, is likely to proceed stereoselectively by participation of the N-phenylcarbamoyl group at O-6 of 6, 11 and 15." @default.
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- W2062824249 date "1994-03-01" @default.
- W2062824249 modified "2023-09-26" @default.
- W2062824249 title "The stereoselective synthesis of cyclomaltopentaose. A novel cyclodextrin homologue with D.P. five" @default.
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- W2062824249 doi "https://doi.org/10.1016/s0040-4039(00)73196-0" @default.
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