13C and1H NMR spectra of biologically active compounds. VII. Diastereomers of 2,2-dialkylspiro[cyclopropane-3,3′-indene]-1-carboxylic acids of the pyrethroid series

1988 ◽  
Vol 24 (4) ◽  
pp. 491-497
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L. M. Khalilov ◽  
V. S. Sultanova ◽  
E. V. Vasil'eva ◽  
L. V. Spirikhin ◽  
I. P. Baikova ◽  
...  
1989 ◽  
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A. A. Fatykhov ◽  
V. S. Sultanova ◽  
F. Z. Makaev ◽  
F. Z. Galin ◽  
...  

1988 ◽  
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L. M. Khalilov ◽  
F. Z. Galin ◽  
E. V. Vasil'eva ◽  
D. B. Amirkhanov ◽  
...  

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L. A. Baltina ◽  
L. V. Spirikhin ◽  
E. V. Vasil'eva ◽  
R. M. Kondratenko ◽  
...  

1991 ◽  
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M. �. Adler ◽  
O. V. Shitikova ◽  
M. S. Miftakhov ◽  
G. A. Tolstikov

1988 ◽  
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U. M. Dzhemilev ◽  
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Roger G. Hall ◽  
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Ashok S. Shyadligeri

AbstractTrifluoromethyl containing heterocycles are an integral part of many biologically active compounds in the agro and pharmaceutical chemistry. Herein, we report an efficient and concise three-step synthesis of 5-halo-6-trifluoromethylpyridine-3-carbonitriles from a trifluoroacetyl vinylogous enamine starting material. Hydrolysis furnishes the carboxylic acids.


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