1,3-DIPOLAR CYCLO-ADDITIONS BETWEEN NITRILE OXIDES AND SUBSTITUTED 7-OXABICYCLO[2.2.1]HEPTENES
1,3-DIPOLAR CYCLO-ADDITIONS BETWEEN NITRILE OXIDES AND SUBSTITUTED 7-OXABICYCLO[2.2.1]HEPTENES
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DOI：
10.1021/jo00286a018
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发表时间：
1989-12-08
影响因子：
3.6
通讯作者：
PLUMET, J
中科院分区：
文献类型：
--
作者：
ARJONA, O;DOMINGUEZ, C;PLUMET, J
双环衍生物，如l1添加软亲电子试剂的区域和立体选择性的方式影响的取代基在C-2;然而，这是不是那么清楚地建立狄尔斯-阿尔德环加成。2因此，这种遥控器似乎是高度依赖反应的。在f大学Complutense。' CSIC。
Bicyclic derivatives such as l1 add soft electrophiles in a regio-and stereoselective manner influenced by the substituents at C-2; however, this is not so clearly established for Diels-Alder cycloadditions. 2 Thus, this remote control appears to be highly reaction dependent. On the f Universidad Complutense.‘CSIC.