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硝酮与螺[5.5]-1-十一烯-3-酮的环加成反应
引用本文:冯亚青,张晓东. 硝酮与螺[5.5]-1-十一烯-3-酮的环加成反应[J]. 天津大学学报(自然科学与工程技术版), 1996, 0(2)
作者姓名:冯亚青  张晓东
作者单位:天津大学制药厂
基金项目:国家教委留学回国人员科研基金
摘    要:(Z)-N一苯基-α-取代苯基硝酮与螺[5.5]-1-十一烯-3-酮的环加成反应,制得一种新的杂螺环及几个螺取代的异唑衍生物,经核磁谱确定只有一种区域选择异构体,两种几何异构体.并对3b进行了x-衍射结构分析,进一步证实了其立体构型.

关 键 词:1.3-偶极环加成,(Z)-N-苯基-α-取代苯基硝酮,螺[5.5]-1-十一烯-3-酮

CYCLOADDITION OF NITRONES TO SPIRO [5.5]UNDEC-1 -EN-3-ONE
Feng Yaqing, Zhang Xiaodong. CYCLOADDITION OF NITRONES TO SPIRO [5.5]UNDEC-1 -EN-3-ONE[J]. Journal of Tianjin University(Science and Technology), 1996, 0(2)
Authors:Feng Yaqing   Zhang Xiaodong
Abstract:A new heterocycle-system and several spiro-substituted isoxazole derivatives were synthesized by 1, 3-dipolar cycloadditions of (Z)-N-phenyl-a-substituted-pheny nitrones to spiro [5. 5]undec-1-en-3-one. NMR studies confirmed that only one regioisomer and two geometrical i-someres were formed selectively. X-ray structure analysis carried out for one 3b of these products shows the occurrence of only one stereoismer.
Keywords:dipolar cycloaddition  (Z)-N-phenyl-a-substituted phenyl nitrones  spiro[5. 5]undec-1-en-3-one  
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