The conversion of a pyrrole trimer derivative into a 4,5,6,7-tetrahydro-4-(pyrrol-2-yl)indol-7-yltosyl-aminoindole

被引:0
|
作者
Zhao, YK [1 ]
Helliwell, M [1 ]
Joule, JA [1 ]
机构
[1] Univ Manchester, Dept Chem, Manchester M13 9PL, Lancs, England
来源
ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY | 2000年 / 56卷
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中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Vilsmeier formylation of trans-1-(4-methylphenylsulfonyl)2,5-bis(pyrrol-2-yl)pyrrolidine leads to cleavage of the central ring then a reclosure resulting in the formation of trans-N-[2-formyl-4-(5-formylpyrrol-2-yl)-4,5,6,7-tetrahydroindol-7-yl]-toluenesulfonamide, C21H21N3O4S.
引用
收藏
页码:714 / 715
页数:2
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