A. Abouabdellah

发表

Stereoselective Synthesis of Peptidyl Trifluoromethyl Alcohols and Ketones: Inhibitory Potency Against Human Leucocyte Elastase, Cathepsin G, Porcine Pancreatic Elastase and HIV‐1 Protease

D. Bonnet-Delpon, J. Bégué, A. Amour, 1998, The Journal of pharmacy and pharmacology.

Synthesis and in vivo antimatarial activity of 12α-trifluoromethyl-hydroartemisinin

D. Bonnet-Delpon, J. Bégué, J. Gantier, 1996 .

New applications of fluorinated building blocks

J. Welch, F. Gyenes, A. Abouabdellah, 1995 .

Optically active fluorinated β-lactam building blocks: A novel fluorinated retroamide isostere.

J. Welch, A. Abouabdellah, 1994 .

A new approach to the synthesis of functionalized pyrido[2,3-b]indoles by way of a palladium-catalyzed ring closing reaction between the N-1 and C-9a positions

R. Dodd, A. Abouabdellah, 1998 .

Lewis acid induced ene cyclization of ω-olefinic trifluoromethyl ketones : access to bicyclic compounds bearing a CF3 group

D. Bonnet-Delpon, J. Bégué, A. Abouabdellah, 1991 .

The selective reversible FAAH inhibitor, SSR411298, restores the development of maladaptive behaviors to acute and chronic stress in rodents

G. Griebel, J. Stemmelin, O. Bergis, 2018, Scientific Reports.

Synthesis and biological activity of novel 3′-trifluoromethyl taxoids

J. Veith, I. Ojima, J. Bégué, 1997 .

Diastereoselective Synthesis of the Nonracemic Methyl syn-(3-Fluoroalkyl)isoserinates

D. Bonnet-Delpon, J. Bégué, A. Abouabdellah, 1997 .

Lewis acid-induced ene-cyclization of ω-olefinic trifluoromethyl ketones: access to alicyclic compounds bearing a CF3 group

D. Bonnet-Delpon, J. Bégué, C. Aubert, 1991 .

Tandem carbonyl ene cyclization-cycloalkylation: a route to trifluoromethyl diterpenoids.

D. Bonnet-Delpon, A. Abouabdellah, 1994 .

Lewis Acid Induced Ene Cyclization of ω‐Olefinic Trifluoromethyl Ketones: Access to Bicyclic Compounds Bearing a CF3 Group.

D. Bonnet-Delpon, J. Bégué, A. Abouabdellah, 1992 .

Trifluoromethyl ketones derived from squalene: inhibition of the cholesterol biosynthesis in HepG2 cells

O. Boutaud, C. Richard, F. Schuber, 2000 .

N-Substituted 4-amino-3,3-dipropyl-2(3H)-furanones: new positive allosteric modulators of the GABA(A) receptor sharing electrophysiological properties with the anticonvulsant loreclezole.

W. Sieghart, E. Sigel, R. Baur, 2002, Journal of medicinal chemistry.

The selective reversible FAAH inhibitor, SSR411298, restores the development of maladaptive behaviors to acute and chronic stress in rodents

G. Griebel, J. Stemmelin, O. Bergis, 2018, Scientific Reports.

First Synthesis of Methyl syn 3-CF3-Isoserinate

D. Bonnet-Delpon, J. Bégué, A. Abouabdellah, 1996 .

Syntheses, Biological Activity, and Conformational Analysis of Fluorine‐Containing Taxoids

S. Kuduk, S. Chakravarty, I. Ojima, 1997 .

Syntheses, Biological Activity, and Conformational Analysis of Fluorine-Containing Taxoids

S. Kuduk, S. Chakravarty, J. Veith, 1996 .