ACS Comb. Sci. 2015, 17 (10), 615-622
DOI: 10.1021/acscombsci.5b00091
Bogolubsky A. V.; Moroz Y. S.; Mykhailiuk P. K.; Pipko S. E.; Zhemera A. V.; Konovets A. I.; Stepaniuk O. O.; Myronchuk I. S.; Dmytriv Y. V.; Doroschuk R. A.; Zaporozhets O. A.; Tolmachev A.
A one-pot parallel synthesis of N1-aryl-N2-alkyl-substituted oxamides with 2,2,2-trifluoroethyl chlorooxoacetate was developed. The synthesis of a library of 45 oxamides revealed higher efficiency of this reagent over the known ethyl chlorooxoacetate. The reagent was successfully used to prepare the known oxamide-containing HIV entry inhibitors.