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Neoglycopeptide synthesis by Suzuki-Miyaura couplings between glycosyl aryl boronic acids and iodopeptides
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نویسنده
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chen g. ,gu x. ,chen l. ,wang x. ,chen y.-l. ,shen j. ,zeng w.
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منبع
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protein and peptide letters - 2014 - دوره : 21 - شماره : 10 - صفحه:1004 -1010
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چکیده
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Suzuki-miyaura coupling reaction was applied in the syntheses of neoglycopeptides. this work utilizes new type of glycosyl aryl boronic acid and readily accessible iodo amino acids/iodopeptides. both carbohydrate and peptide moieties are unprotected and the final product could be isolated directly. the neoglyco amino acid and neoglycopeptide products feature an o-glycosyl biaryl linker between the carbohydrate and peptide moieties. © 2014 bentham science publishers.
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کلیدواژه
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Glycopeptides; Glycosyl aryl boronic acids; Iodo peptides; Neoglycopeptides; Suzuki-Miyaura coupling
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آدرس
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school of pharmacy,china pharmaceutical university,24 tongjiaxiang, China, school of pharmacy,china pharmaceutical university,24 tongjiaxiang,nanjing,china,shanghai institute of materia medica,chinese academy of sciences,555 zuchongzhi road, China, shanghai institute of materia medica,chinese academy of sciences,555 zuchongzhi road, China, shanghai institute of materia medica,chinese academy of sciences,555 zuchongzhi road, China, shanghai institute of materia medica,chinese academy of sciences,555 zuchongzhi road, China, shanghai institute of materia medica,chinese academy of sciences,555 zuchongzhi road, China, school of pharmaceutical sciences,central south university,172 tongzipo road, China
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Authors
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