REACTIONS OF N-PYRROLIDINOCYCLOALKENES WITH 2-PHENYL-4-BENZYLIDENE-5-OXAZOLONE

被引：0
|
作者：
KUMARI, AS [1 ]
机构：
[1] INDIAN INST CHEM TECHNOL, HYDERABAD, INDIA
来源：
INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY | 1994年 / 33卷 / 04期
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D O I：
暂无
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Novel 3alpha-benzamido-bicyclo[3.3.1]nonane-2, 9-dione (8) and tetrahydro-1-azaindan-3-ones (6, 7, 9 and 10) have been obtained from the reactions of N-pyrrolidinocyclopentene (1), N-pyrrolidinocyclohexene (2), N-pyrrolidinocycloheptene (3) and N-pyrrolidinocyclooctene (4) with the heterocyclic substrate 2-phenyl-4-benzylidene-5-oxazolone (5). A plausible pathway has been proposed.
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页码：385 / 386
页数：2
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