The formation of O-glycosidic linkage is arguably one of the most important topics in glycoscience due to the prevalence of O-glycosides in nature. Great efforts have been devoted to this field by many carbohydrate chemists to develop stereoselective/stereospecific glycosylation methodologies. Although glycosyl donor- and acceptor-controlled strategies have significantly progressed, the tedious design and pre-synthesis of substrates could not be avoided. On the other hand, reagent-controlled glycosylation can overcome these challenges and produce the desired selectivity by only altering external factors such as concentration, reagents or other reaction conditions. This mini-review discusses selected recent novel methodologies on reagent-mediated stereo-controlled glycosylation in the last decade, classified by the types of glycosyl donors.
机构:
Kobe Pharmaceut Univ, Dept Organ Chem Life Sci, Higashinada Ku, Kobe, Hyogo 6588558, JapanKobe Pharmaceut Univ, Dept Organ Chem Life Sci, Higashinada Ku, Kobe, Hyogo 6588558, Japan
Okitsu, Takashi
Sato, Kana
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Kobe Pharmaceut Univ, Dept Organ Chem Life Sci, Higashinada Ku, Kobe, Hyogo 6588558, JapanKobe Pharmaceut Univ, Dept Organ Chem Life Sci, Higashinada Ku, Kobe, Hyogo 6588558, Japan
Sato, Kana
Wada, Akimori
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Kobe Pharmaceut Univ, Dept Organ Chem Life Sci, Higashinada Ku, Kobe, Hyogo 6588558, JapanKobe Pharmaceut Univ, Dept Organ Chem Life Sci, Higashinada Ku, Kobe, Hyogo 6588558, Japan