N-Trifluoroacetyl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline ozonides

被引：0

作者：

A. G. Tolstikov

R. G. Savchenko

D. V. Nedopekin

S. R. Afon’kina

E. S. Lukina

V. N. Odinokov

机构：

[1] Russian Academy of Sciences,Institute of Petrochemistry and Catalysis

来源：

Russian Chemical Bulletin | 2011年 / 60卷

关键词：

cycloaddition; cyclopentadiene; imines; 3a,4,5,9b-tetrahydro-3; -cyclo-penta[; ]quinolines; trifluoroacetamides; ozonolysis; ozonides; the Povarov reaction;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

A three-component condensation of aromatic amine, aldehyde, and cyclopentadiene with subsequent N-trifluoroacetylation leads to 4- and 4,8-substituted N-trifluoroacetyl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinolines. Ozonation of the double bond in the latter produced the corresponding isomeric stable ozonides having (1R*,4S*,5aR*,6S*,11bR*)-configuration and differing in inversion at the carboxamide nitrogen atom.

引用

页码：160 / 167

页数：7

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