Rufine Akué-Gédu

发表

Use of copper(I) catalyzed azide alkyne cycloaddition (CuAAC) for the preparation of conjugated pyrrolo[2,3-a]carbazole Pim kinase inhibitors.

A. Gautier, M. El-ghozzi, P. Koskinen, 2012, European journal of medicinal chemistry.

Kinase inhibitory potencies and in vitro antiproliferative activities of N-10 substituted pyrrolo[2,3-a]carbazole derivatives.

E. Débiton, P. Moreau, F. Anizon, 2012, Bioorganic & medicinal chemistry letters.

Studies on pyrrolidinones. Synthesis of 4,5-fused-3-hydroxypyridinyl-2-propionic acid derivatives

J. Hénichart, B. Rigo, L. Hijfte, 2012 .

On the synthesis of 5‐ethyl meldrum's acid

B. Rigo, D. Couturier, Rufine Akué-Gédu, 2006 .

Synthesis of 2-pyrone-4-carboxaldehydes from acetylene dicarboxaldehyde monoacetal

J. Hénichart, B. Rigo, D. Couturier, 2004 .

Studies on pyrrolidinones. On the decarboxylation of pyroglutamic acids and N-acyl prolines in acidic media

B. Decroix, B. Rigo, M. Debacker, 2002 .

Studies on pyrrolidones. An improved synthesis of N-arylmethyl pyroglutamic acids

J. Hénichart, B. Rigo, D. Couturier, 2003 .

Studies on pyrrolidinones: a reaction of methylene dichloride under Friedel–Crafts conditions. Synthesis of an α-hydroxymethyl ketone in the hexahydrobenzo[f]indolizine series

J. Hénichart, B. Rigo, A. Bourry, 2004 .

Corrigendum to “Large scale synthesis of acetylene dicarboxaldehyde mono and diacetal”: [Tetrahedron Lett. 45 (2004) 1829]

B. Rigo, Rufine Akué-Gédu, 2005 .

Large scale synthesis of acetylene dicarboxaldehyde mono and diacetal

B. Rigo, Rufine Akué-Gédu, 2004 .

Studies on pyrrolidinones. synthesis of fused 1,5-naphthyridines

J. Hénichart, B. Rigo, L. Hijfte, 2012 .

Allylic dehydration, retro-pinacol, pinacol-like and enamide reactions: Synthesis of new isoquinolines

B. Norberg, F. Durant, B. Rigo, 2004 .

Synthesis, kinase inhibitory potencies, and in vitro antiproliferative evaluation of new Pim kinase inhibitors.

Stefan Knapp, Panagis Filippakopoulos, Jenny Bain, 2009, Journal of medicinal chemistry.

Synthesis and Biological Activities of 4‐Substituted Pyrrolo[2,3‐a]carbazole Pim Kinase Inhibitors.

E. Débiton, P. Moreau, F. Anizon, 2013 .

Synthesis and biological activities of aminopyrimidyl-indoles structurally related to meridianins.

L. Meijer, M. Prudhomme, E. Débiton, 2009, Bioorganic & medicinal chemistry.

8,8′-Dichloro-1,1′,5,5′-tetrahydro-10,10′-bipyrrolo[1,2-b]isoquinoline-3,3′(2H,2′H)-dione

B. Norberg, F. Durant, B. Rigo, 2003 .

Alkyne via Solid‐Liquid Phase‐Transfer Catalyzed Dehydrohalogenation: Acetylene Dicarboxaldehyde Tetramethyl Acetal and Acetylene Dicarboxaldehyde Dimethyl Acetal

B. Rigo, Rufine Akué-Gédu, 2005 .

Synthesis, Pim kinase inhibitory potencies and in vitro antiproliferative activities of diversely substituted pyrrolo[2,3-a]carbazoles.

P. Cohen, J. Bain, P. Moreau, 2010, Bioorganic & Medicinal Chemistry.

Synthesis and biological activities of 4-substituted pyrrolo[2,3-a]carbazole Pim kinase inhibitors.

E. Débiton, P. Moreau, F. Anizon, 2012, European journal of medicinal chemistry.