A novel deacylation during the amination of trifluoromethyl β-dicarbonyl compounds
S Fioravanti, L Pellacani, F Ramadori, PA Tardella
Index: Fioravanti, Stefania; Pellacani, Lucio; Ramadori, Federico; Tardella, Paolo A. Tetrahedron Letters, 2007 , vol. 48, # 44 p. 7821 - 7824
Full Text: HTML
Citation Number: 14
Abstract
Starting from trifluoromethyl β-dicarbonyl compounds, a rare loss of CF3CO was observed in the amination reactions performed under heterogeneous conditions using NsONHCO2Et as the aminating agent and CaO or NaH as the base, while corresponding nonfluorinated β- dicarbonyl compounds under analogous conditions give non deacylated aminated compounds. This reaction can facilitate a direct synthesis of N-substituted α-amino esters ...
Related Articles:
[Barcelo, Gerard; Senet, Jean-Pierre; Sennyey, Gerard; Bensoam, Jean; Loffet, Albert Synthesis, 1986 , # 8 p. 627 - 632]
RESEARCHES ON HYDANTOINS. XLIII. SYNTHESIS OF THE POLYPEPTIDE-HYDANTOIN:“HYDANTOIN-3-ACETIC ACID” 1
[Johnson; Renfrew Journal of the American Chemical Society, 1925 , vol. 47, p. 244]
[Kantlehner, Willi; Maier, Thomas; Loeffler, Wolfgang; Kapassakalidis, Joanis J. Liebigs Annalen der Chemie, 1982 , # 3 p. 507 - 529]
[Kantlehner, Willi; Maier, Thomas; Loeffler, Wolfgang; Kapassakalidis, Joanis J. Liebigs Annalen der Chemie, 1982 , # 3 p. 507 - 529]
RESEARCHES ON HYDANTOINS. XLIII. SYNTHESIS OF THE POLYPEPTIDE-HYDANTOIN:“HYDANTOIN-3-ACETIC ACID” 1
[Johnson; Renfrew Journal of the American Chemical Society, 1925 , vol. 47, p. 244]