REACTIONS OF POLYFLUOROCARBONYL COMPOUNDS WITH 1,3,3-TRIMETHYL-3,4-DIHYDROISOQUINOLINE AND ITS DERIVATIVES

被引:13
作者
SVIRIDOV, VD
CHKANIKOV, ND
GALAKHOV, MV
SHKLYAEV, YV
SHKLYAEV, VS
ALEKSANDROV, BB
GAVRILOV, MS
机构
[1] A. N. Nesmeyanov Institute of Heteroorganic Compounds, Academy of Sciences of the USSR, Moscow
来源
BULLETIN OF THE ACADEMY OF SCIENCES OF THE USSR DIVISION OF CHEMICAL SCIENCE | 1990年 / 39卷 / 06期
关键词
D O I
10.1007/BF00962396
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
1,3,3-Trimethyl-3,4-dihydroisoquinolines, which exist in the imine form, undergo C-hydroxyalkylation upon reaction with hexafluoroacetone and esters of trifluoropyruvic acid at the C1-CH3 group at 20-degrees-C. The products with the ketoesters are converted upon heating to gamma-lactams. Derivatives of 1,3,3-trimethyl-3,4-dihydroisoquinoline substituted at C1-CH3 group and existing in the enamine form, react with esters of trifluoropyruvic acid at 20-degrees-C to give exclusively gamma-lactams and do not give reaction products with hexafluoroacetone.
引用
收藏
页码:1268 / 1272
页数:5
相关论文
共 3 条
[1]  
CHKANIKOV ND, 1990, IZV AKAD NAUK SSSR K, P383
[2]  
SVIRIDOV VD, 1986, IZV AKAD NAUK SSSR K, P1915
[3]  
Zelenin A. E., 1986, IAN SSSR KH, P2074