Reaction of 2-formyl-1,3-cyclanediones with N,N′-substituted 1,1-diamino-2-nitroethylenes

被引：0

作者：

Strakov A.Ya. ^{[1
]}

Petrova M.V. ^{[1
]}

Gurkovskii A.I. ^{[1
]}

Neiland O.Ya. ^{[1
]}

机构：

[1] Riga Technical University

来源：

Chemistry of Heterocyclic Compounds | 1999年 / 35卷 / 3期

关键词：

Indanedione; Organic Chemistry; Cyclohexanediones; Quinoline; Nitroethylenes;

D O I：

10.1007/BF02259356

中图分类号：

学科分类号：

摘要：

Reaction of 2-formyldimedone and 2-formyl-1,3-indanedione with 1,1-di(2-hydroxyethylamino)- and 1,1-di(4-morpholyl)-2-nitroethylenes produces 2-[3,3-di(2-hydroxyethylamino)-2-nitroprop-2-en-1-ylidene]- and 2-[3,3-di(4-morpholyl)-2-nitroprop-2-en-1-ylidene]-5,5-dimethyl-1, 3-cyclohexanediones and the 1,3-indanediones, respectively. The reaction of the same 2-formyl-1,3-cyclanediones with 2-nitromethyleneimidazolidine yields 8,8-dimethyl-4-nitro-6-oxo-1,2,3,6,7,8-hexahydroimidazo[1,2-a]quinoline and 4-nitro-6-oxo-1,2-dihydro-6H-imidazo[1,2-c]-4-azafluorene. ©1999 KluwerAcademic/Plenum Publishers.

引用

页码：286 / 289

页数：3

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