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作 者:Zai Ming ZHU Yin WANG Yong Ting XU n Min MEl(Department of Chemistry. Linoning Normal University, Daljan. 116029)Qun LIU(Department of Chemistry, Northeast Normat University, Changchun. 130024)Jie Han HU(Dalian lnstitute of Chemital Phrrfor, Atalemin-Si
出 处:《Chinese Chemical Letters》1997年第5期367-368,共2页中国化学快报(英文版)
摘 要:α, α′ -Dioxo (ester ) ketene cyclic S, S-acetais 2 were reacted withethyleneddriine to chrd α, α′-dioxo (ester)ketene cyclic N, N-acetals 3 Thisprocess provides a new method for the synthesis of 3 in gnd yteld under mildcondition. All products are confirmed with elementai analpeis, IR, 1H NMR and13~C NMRα, α′ -Dioxo (ester ) ketene cyclic S, S-acetais 2 were reacted withethyleneddriine to chrd α, α′-dioxo (ester)ketene cyclic N, N-acetals 3 Thisprocess provides a new method for the synthesis of 3 in gnd yteld under mildcondition. All products are confirmed with elementai analpeis, IR, 1H NMR and13~C NMR
关 键 词:Reaction of ester)ketene Cyclic S S-Acetals with Ethylenediamine Oxoketene Cyclic S S-Acetals Chemistry Dioxo
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