Synthesis of unusual trifluoromethylated amino acids is described. Csp3-H functionalization of alkyl group directly attached to aromatic ring with a-iminoesters via electrophilic aminoalkylation is a viable approach for the synthesis of trifluoromethylated amino acids. The synthesis of racemic amino acids was achieved using catalytic amount of triflic acid under mild reaction conditions
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A series of novel (1-aminoalkyl)(trifluoromethyl)- and -(difluoromethyl)phosphinic acids – analogues...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
Osipov SN, Kolomiets AF, Fokin AV, Burger K, Sewald N. Synthesis of alpha-Trifluoromethyl Substitute...
International audienceAn efficient route to new α-CF3-α-amino acid derivatives bearing an arylalkyny...
Six new N-protected amino acid trifluoroethyl esters were synthesized by the catalysis of 4-dimethyl...
Addition of a Reformatsky reagent to α-aryl(alkyl) α-trifluoromethyl <i>N</i>-<i>tert</i>-butanesul...
When fluorine is incorporated into organic molecules, the C-F bond participates in a variety of ster...
International audienceFluoroalkyl amino reagents 1a and 2a have been developed from commercially ava...
International audienceThe diastereoselective addition of allyl zinc and allylindium derivatives to α...
Mentor: Dr. John GituaAmino acids are important biological compounds and useful chemical reagents in...
Fluoroalkyl amino reagents <b>1a</b> and <b>2a</b> have been developed from commercially available t...
Backbone-homologated amino acids have been synthesized, containing three vicinal fluorine atoms plac...
A novel method for the synthesis of chiral α-amino acids has been developed where the acid functiona...
A novel route has been developed for the solid-phase synthesis of N-carboxyalkyl unnatural amino aci...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A series of novel (1-aminoalkyl)(trifluoromethyl)- and -(difluoromethyl)phosphinic acids – analogues...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
Osipov SN, Kolomiets AF, Fokin AV, Burger K, Sewald N. Synthesis of alpha-Trifluoromethyl Substitute...
International audienceAn efficient route to new α-CF3-α-amino acid derivatives bearing an arylalkyny...
Six new N-protected amino acid trifluoroethyl esters were synthesized by the catalysis of 4-dimethyl...
Addition of a Reformatsky reagent to α-aryl(alkyl) α-trifluoromethyl <i>N</i>-<i>tert</i>-butanesul...
When fluorine is incorporated into organic molecules, the C-F bond participates in a variety of ster...
International audienceFluoroalkyl amino reagents 1a and 2a have been developed from commercially ava...
International audienceThe diastereoselective addition of allyl zinc and allylindium derivatives to α...
Mentor: Dr. John GituaAmino acids are important biological compounds and useful chemical reagents in...
Fluoroalkyl amino reagents <b>1a</b> and <b>2a</b> have been developed from commercially available t...
Backbone-homologated amino acids have been synthesized, containing three vicinal fluorine atoms plac...
A novel method for the synthesis of chiral α-amino acids has been developed where the acid functiona...
A novel route has been developed for the solid-phase synthesis of N-carboxyalkyl unnatural amino aci...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A series of novel (1-aminoalkyl)(trifluoromethyl)- and -(difluoromethyl)phosphinic acids – analogues...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...