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• W3171726375 abstract "An efficient synthetic strategy has been developed for the synthesis of a tetrasaccharide related to the O-specific polysaccharide from Escherichia coli O132 as their 2-aminoethyl glycosides in a very good yield by adopting sequential glycosylation followed by in-situ removal of the p-methoxybenzyl (PMB) group in the same reaction pot. Furthermore, the synthetic route was adapted by carrying out three stereoselective iterative glycosylations followed by in situ removal of the PMB group in one pot. The stereochemical outcomes of all the glycosylation steps were excellent with satisfactory yields." @default.
• W3171726375 created "2021-06-22" @default.
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• W3171726375 date "2021-03-31" @default.
• W3171726375 modified "2023-09-23" @default.
• W3171726375 title "One-pot iterative glycosylations toward a tetrasaccharide related to the O-specific polysaccharide from Escherichia coli O132" @default.
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• W3171726375 doi "https://doi.org/10.1080/07328303.2021.1928153" @default.
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