Transformations of stereoisomeric 2-chloro-3-R-pentane-1,5-diones in reaction with phenylhydrazine

被引：2

作者：

Moskovkina, T. V. ^{[1
]}

Kalinovskii, A. I.

机构：

[1] Far Eastern State Univ, Vladivostok 690600, Russia

[2] Russian Acad Sci, Pacific Inst Bioorgan Chem, Far Eastern Div, Vladivostok, Russia

来源：

RUSSIAN JOURNAL OF ORGANIC CHEMISTRY | 2007年 / 43卷 / 02期

关键词：

D O I：

10.1134/S1070428007020108

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Monophenylhydrazones were prepared from three monochloro derivatives of arylaliphatic 1,5-diketones, and some their transformations were investigated. The monophenyihydrazones formed regiospecifically, and the direction of the reaction was governed by the substituent attached to C-3 atom in the initial chlorodiketones. C Formerly unknown products of transformations suffered by monophenylhydrazones obtained were described: 2-amino-1,3-diphenyl-3-(2-phenylindolyl-3)-propan-1-one, 3-benzoyl-2,4,6-triphenl-2,3,4,5-tetrahydropyridazine, and 3-methyl-1,5-diphenyl-5-phenylazopent-4-en-1-one.

引用

页码：214 / 219

页数：6