📜2-Deoxy-2-Acetamido-3,4,6-Tri-O-Acetyl-D-Glucopyranose置于1H-1,2,4-三唑,三氟甲磺酸三甲基硅酯,双氧水体系中,用 硝基甲烷,二氯甲烷 用作溶剂,化学反应 15.0H,反应生成己基-2,3,4,6-四-氧-乙酰基-β-D-吡喃葡萄糖苷
参考文献:New α-Selective Thermal Glycosylation Of Acetyl-Protected 2-Acetamido-2-Deoxy-β-D-Glucopyranosyl Diphenylphosphinate
标题:New α-Selective Thermal Glycosylation Of Acetyl-Protected 2-Acetamido-2-Deoxy-β-D-Glucopyranosyl Diphenylphosphinate
摘要:This Paper Describes New Alpha-Selective Thermal Glycosylation Using Acetyl-Protected 2-Acetamido-2-Deoxy-Beta-D-Glucopyranosyl Diphenylphosphinate (4) As A Glycosyl Donor. When The Glycosylation Of 4 With 1-Hexanol Was Carried Out Under Various Conditions,The Conditions Using Trimethylsilyl Trifluoromethanesulfonate As A Promoter In Nitromethane At Reflux Temperature Were Most Suitable For The Formation Of The Alpha Anomer. The Glycosylation Of 4 With The Other Common Alcohols Gave Corresponding Alpha-Glycosides In Relatively High Yields Under The Conditions. When Cholesterol,A Very Steric Hindered Alcohol,Was Used As A Glycosyl Acceptor,Alpha-Glycoside Was Also Produced Predominantly. (C) 2000 Elsevier Science Ltd. All Rights Reserved.
Doi:10.1016/s0008-6215(00)00069-0