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Fluoroalkylated α,β-unsaturated imines as synthons for the preparation of fluorinated triazinane-2,4-diones and dihydropyrimidin-2(1H)-ones.

Authors :
Fernández de Trocóniz G
Ochoa de Retana AM
Rubiales G
Palacios F
Source :
The Journal of organic chemistry [J Org Chem] 2014 Jun 06; Vol. 79 (11), pp. 5173-81. Date of Electronic Publication: 2014 May 13.
Publication Year :
2014

Abstract

A regioselective addition of isocyanates to fluoroalkylated α,β-unsaturated imines 1 is described. Fluoroalkyl-substituted triazinane-2,4-diones 4 are obtained by the reaction of phenyl isocyanate with fluorinated imines 1, while fluorinated dihydropyridin-2(1H)-ones 7 are prepared when tosyl isocyanate is used. Tetrahydro-pyridin-2(1H)-one 10 is obtained by catalytic reduction of dihydropyridin-2(1H)-one 7. Computational studies are performed to explain the different behaviors of both isocyanates and the mechanisms of the processes.

Details

Language :
English
ISSN :
1520-6904
Volume :
79
Issue :
11
Database :
MEDLINE
Journal :
The Journal of organic chemistry
Publication Type :
Academic Journal
Accession number :
24803029
Full Text :
https://doi.org/10.1021/jo500745u