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作 者:Zhan Jiang LI Li Ben WANG and Zhi Tang HUANG(Institute of Chemistry. Academia Sinica. Beijing 100080)
出 处:《Chinese Chemical Letters》1995年第3期185-188,共4页中国化学快报(英文版)
摘 要:Heterocyclic ketene aminals 1 or 2 reacted with 2.3. 4. 6-tetra-O-acetyl-α-D-glucopyranosyl bromide using mercuric cyanide-calcium hydride or mercuric cyanide-molecular sieve 4A as catalyst to give the O-glycosidated heterocyclic ketene aminals 3 or 4 in moderate yields.Heterocyclic ketene aminals 1 or 2 reacted with 2.3. 4. 6-tetra-O-acetyl-α-D-glucopyranosyl bromide using mercuric cyanide-calcium hydride or mercuric cyanide-molecular sieve 4A as catalyst to give the O-glycosidated heterocyclic ketene aminals 3 or 4 in moderate yields.
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