6-Tri- and 6-difluoromethylcomanic acids and their ethyl esters reacted with aminoguanidine, predominantly giving 5-RF-pyrazolo[1,5-c] pyrimidines, whereas the reaction of the openchain synthetic equivalents, i.e., ethyl 7,7,7-trifluoro- and 7,7-difluoro-2,4,6-trioxoheptanoates, with this polynucleophile allowed us to obtain regioselectively 2-RF- pyrazolo[1,5-c]pyrimidines. © 2012 Springer Science+Business Media New York
Two facile and efficient one-step procedures for the regioselective synthesis of 7-aryl-5-methyl- an...
A facile synthesis of 7-amino-5-chloro-3-B-D-ribofuranosyl-pyrazolo[4,3-d]pyrimidine (5-chlorofonnyc...
Diversity oriented syntheses of some furo[2,3-d]pyrimidines and pyrrolo[2,3-d] pyrimidines related t...
International audienceA novel two-step synthesis of trifluoromethylated 3,5-disubstituted pyrazolo[1...
Some compounds, analogous to those found in naturally occurring systems, are found to possess chemo...
AbstractA regioselective synthesis of 3-trifluoromethyl-1-phenyl-1H-pyrazoles (1,3-isomers) as well ...
© 2015 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. A method...
Pyrazolo[1,5-c]pyrimidines are biologically active, synthetically useful and important heterocyclic ...
International audienceA simple and efficient method for synthesis of 5,7-disubstituted pyrazolo[1,5-...
A number of trifluoromethylated 3-(pyrazolyl)indoles was synthesized from 2-(trifluoromethyl)comanic...
Abstract – Trifluoromethyl group substituted pyrazole derivatives were prepared from hydrazines and ...
Chapter 1 introduces the modem pharmaceutical industry in terms of the drug discovery process leadin...
A new carbon–carbon bond cleavage reaction was developed for the efficient synthesis of multisubstit...
AbstractAn easy and efficient route for the synthesis of some tetrazolo[1,5-a]-, pyrazolo[1,5-a]- an...
The pyrazolo[1,5-a]pyrimidine structural motif may be found in a large number of pharmaceutical agen...
Two facile and efficient one-step procedures for the regioselective synthesis of 7-aryl-5-methyl- an...
A facile synthesis of 7-amino-5-chloro-3-B-D-ribofuranosyl-pyrazolo[4,3-d]pyrimidine (5-chlorofonnyc...
Diversity oriented syntheses of some furo[2,3-d]pyrimidines and pyrrolo[2,3-d] pyrimidines related t...
International audienceA novel two-step synthesis of trifluoromethylated 3,5-disubstituted pyrazolo[1...
Some compounds, analogous to those found in naturally occurring systems, are found to possess chemo...
AbstractA regioselective synthesis of 3-trifluoromethyl-1-phenyl-1H-pyrazoles (1,3-isomers) as well ...
© 2015 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. A method...
Pyrazolo[1,5-c]pyrimidines are biologically active, synthetically useful and important heterocyclic ...
International audienceA simple and efficient method for synthesis of 5,7-disubstituted pyrazolo[1,5-...
A number of trifluoromethylated 3-(pyrazolyl)indoles was synthesized from 2-(trifluoromethyl)comanic...
Abstract – Trifluoromethyl group substituted pyrazole derivatives were prepared from hydrazines and ...
Chapter 1 introduces the modem pharmaceutical industry in terms of the drug discovery process leadin...
A new carbon–carbon bond cleavage reaction was developed for the efficient synthesis of multisubstit...
AbstractAn easy and efficient route for the synthesis of some tetrazolo[1,5-a]-, pyrazolo[1,5-a]- an...
The pyrazolo[1,5-a]pyrimidine structural motif may be found in a large number of pharmaceutical agen...
Two facile and efficient one-step procedures for the regioselective synthesis of 7-aryl-5-methyl- an...
A facile synthesis of 7-amino-5-chloro-3-B-D-ribofuranosyl-pyrazolo[4,3-d]pyrimidine (5-chlorofonnyc...
Diversity oriented syntheses of some furo[2,3-d]pyrimidines and pyrrolo[2,3-d] pyrimidines related t...