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1,3-偶极环加成合成双-4,5-二氢-1,2,4-噁二唑啉衍生物 被引量:2

Synthesis of Bis-4,5-dihydro-1,2,4-oxadiazoline Derivatives by 1,3-Diplor Cycloaddition
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摘要 用2-苯基-1,2,3-三唑基-4-甲醛(1)或喹喔啉基-2-甲醛(2)与乙二胺缩合成双席夫碱3或4,然后与α-氯代肟在三乙胺条件下发生1,3-偶极环加成得到双-4,5-二氢-1,2,4-噁二唑啉衍生物6a~6f或7a~7f.目标化合物的结构经元素分析,IR,1HN MR和MS确认. Condensation of ethylenediamine with 2-phenyl- 1,2,3-triazole-4-carboxaldehyde (1) or quinoxa- line-2-carboxaldehyde (2) gave bis-Schiff base 3 or 4, which then reacted with a-chloro-oximes to afford bis- bis-4,5-dihydro-1,2,4-oxadiazoline derivatives 6a-6f or 7a-7f by 1,3-dipolar cycloaddition. The structures of new compounds were confirmed by elemental analysis, IR, ^1H NMR and MS spectra.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2007年第9期1162-1166,共5页 Chinese Journal of Organic Chemistry
基金 国家自然科学基金(No20562011) 新疆大学青年启动基金资助项目
关键词 喹喔啉-2-甲醛 2-苯基-1 2 3-三唑基-4-甲醛 双席夫碱 1 3-偶极环加成 双-4 5-二氢-1 2 4-噁二唑啉衍生物 qinoxaline-2-carboxaldehyhyde 2-phenyl-1,2,3-triazole-4-carboxaldehyde bis-Schiff base 1,3-dipolar cycloaddition bis-4,5-dihydro- 1,2,4-oxadiazoline derivative
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