1,3-DIPOLAR CYCLOADDITION REACTIONS OF A HETEROCYCLIC NITRONE

被引:17
作者
ALI, SA
ALMUALLEM, HA
机构
[1] Chemistry Department, King Fahd University of Petroleum and Minerals, Dhahran
关键词
D O I
10.1016/S0040-4020(01)89025-6
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A study of the regio- and stereo-chemical behaviour of the 1,3-dipolar cycloaddition of a series of alkenes with 5,6-dihydro-1,4-oxazine 4-oxide (1) has been carried out. Stereoselectivity in these cycloadditions has been explained in terms of steric factors and secondary orbital interactions. The ratio of the trans and cis conformers of the cycloaddition products has been determined. The nitrone (1) was found to be more reactive than its carbocyclic counterparts.
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页码:5273 / 5282
页数:10
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