摘要
本文通过苯磺酞基α,β-不饱和酮与环成一烯的环加成反应,探讨了苯磺酞基α,β-不饱和酮在Lewis酸催化和无催化剂的条件下发生环加成反应的活性;合成了6-取代-5-(苯磺酰基乙酰基)二环[2.2.1]]庚-2-烯(3)的环加成产物,并对其波谱特性进行了解析.
In this paper 6-Substituent-5-(Phenylsulfonylaetyl)bicyclo[2.2.1]Hept-2-enes were synthesized by Diels-Alder reactions of Phenylsulfonyl α,βunsaturated ketones with cyclopentadiene(Substituent:R=CH3,n-Pr,Ph,H).Their structures were characterized by 1HNMR,IR,MS and elementary analysis.The reaction activities of dienophiles were studed in the presence of Lewis acid or in the absence of catalyst.
出处
《延边大学学报(自然科学版)》
CAS
1997年第3期37-40,49,共5页
Journal of Yanbian University(Natural Science Edition)
关键词
苯磺酰基
不饱和酮
环戊二烯
活性
环加成反应
Phenysulfonyl
Unstaturated ketones
Cyclopentadiene
Cycloadduction
Activity