C. Cavé

发表

Asymmetric Michael reaction involving chiral imines/secondary enamines: stereocontrolled synthesis of 2,2-disubstituted tetrahydrothiophen-3-ones.

G. Morgant, D. Desmaële, J. D'angelo, 2004, Organic letters.

EVALUATION OF IN VITRO ANTIPLASMODIAL ACTIVITY OF ICACINA OLIVIFORMIS’S (STEMS AND ROOTS) AND SPONDIAS PURPUREA’S (LEAVES, BARKS AND ROOTS) EXTRACTS FROM ZIGUINCHOR, SENEGAL

A. Gassama, O. Sambou, S. Cojean, 2019 .

Synthetic approaches to Cinchona alkaloids: the C-8/C-9 disconnection strategy

G. Morgant, J. D'angelo, C. Cavé, 2003 .

Regio- and diastereocontrolled preparative oxidation of methyloctalones by a biomimetic porphyrin catalyst.

P. Vérité, O. Lafont, C. Cavé, 2004, Chirality.

Molecular mechanisms in Alzheimer's disease and related potential treatments such as structural target convergence of antibodies and simple organic molecules.

B. Roques, H. Galons, C. Cavé, 2022, European journal of medicinal chemistry.

Synthesis and Antimalarial Activity of 1,4-Disubstituted Piperidine Derivatives

A. Gassama, S. Cojean, C. Cavé, 2020, Molecules.

Regioselective Annulation of 1,5‐Diketones: Access to Functionalized Hagemann’s Esters

A. Gassama, J. D'angelo, C. Cavé, 2000 .

Simple and efficient synthesis of $$5'$$5′-aryl-$$5'$$5′-deoxyguanosine analogs by azide-alkyne click reaction and their antileishmanial activities

P. Loiseau, C. Cavé, K. Leblanc, 2016, Molecular Diversity.

New Ursolic and Betulinic Derivatives as Potential Cytotoxic Agents

B. Chauffert, M. Lacaille‐Dubois, C. Cavé, 2003, Journal of enzyme inhibition and medicinal chemistry.

The asymmetric Michael-type alkylation of chiral β-enamino esters: critical role of a benzyl ester group in the racemization of adducts

J. D'angelo, Sandrine Delarue-Cochin, C. Cavé, 2005 .

Racemization processes at a quaternary carbon center in the context of the asymmetric Michael reaction

R. Álvarez, J. D'angelo, C. Cavé, 2001 .

Synthesis of Ursolic Phosphonate Derivatives as Potential Anti-HIV Agents

C. Vita, C. Cavé, S. Deng, 2007 .

Asymmetric Michael reaction: novel efficient access to chiral β-ketophosphonates

P. Stephens, Sandrine Delarue-Cochin, C. Cavé, 2007 .

Asymmetric reduction of β-ketoesters and chiral β-iminoesters: impact of a α-quaternary stereocenter.

Sandrine Delarue-Cochin, C. Cavé, D. Joseph, 2011, Chirality.

NEW POLYMER-SUPPORTED CATALYSTS DERIVED FROM CINCHONA ALKALOIDS : THEIR USE IN THE ASYMMETRIC MICHAEL REACTION

R. Álvarez, J. D'angelo, P. Chaminade, 1999 .

SYNTHESIS AND ANTIMALARIAL ACTIVITY OF CINNAMIC ACID DERIVATIVES

A. Gassama, S. Cojean, C. Cavé, 2019 .

Easy access to optically active Hagemann's esters

C. Cavé, R. Jankowski, M. Nour, 2001 .

Methyl methacrylate as acceptor in the asymmetric Michael reaction using chiral β-enaminoesters: Simultaneous, complete stereocontrol of a quaternary carbon center and a tertiary one in the β-position

J. D'angelo, C. Cavé, A. Guingant, 1995 .

Synthesis of phosphonodipeptide conjugates of ursolic acid and their homologs

C. Cavé, S. Deng, M. Nour, 2008 .

ANTIPLASMODIAL ACTIVITY OF EXTRACTS OF KHAYA SENEGALENSIS (DERS.) A. JUS (MELIACEAE) AND MELIA AZEDARACH L., PLANTS OF SENEGALESE TRADITIONAL MEDICINE

A. Gassama, S. Cojean, C. Cavé, 2018 .

A review of natural and modified betulinic, ursolic and echinocystic acid derivatives as potential antitumor and anti-HIV agents.

M. Lacaille‐Dubois, C. Cavé, K. Tan, 2003, Mini reviews in medicinal chemistry.

In vitro identification of imidazo[1,2-a]pyrazine-based antileishmanial agents and evaluation of L. major casein kinase 1 inhibition.

P. Le Pape, B. Baratte, N. Rachidi, 2020, European journal of medicinal chemistry.

Asymmetric Michael reaction between a chiral α,β-dimethyl-β-enamino ester and α-substituted acrylates

G. Morgant, C. Cavé, F. Hendra, 2004 .

α-Thiosubstituted chiral imines/secondary enamines: their use in the asymmetric Michael reaction

D. Desmaële, J. D'angelo, C. Cavé, 2000 .

Stereocontrolled approach to quinuclidine derivatives

J. D'angelo, C. Cavé, A. D. S. Goes, 1998 .

A new asymmetric bridging annulation reaction involving the intramolecular michael addition of chiral imines to enoates

J. D'angelo, C. Cavé, A. Chiaroni, 1994 .

Stereochemical Aspects in the Asymmetric Michael Addition of Chiral Imines to Substituted Electrophilic Alkenes.

D. Desmaële, J. D'angelo, C. Cavé, 1996, The Journal of organic chemistry.

GDP-Mannose Pyrophosphorylase: A Biologically Validated Target for Drug Development Against Leishmaniasis

T. Ha-Duong, P. Loiseau, C. Cavé, 2019, Front. Cell. Infect. Microbiol..

Biochemical analysis of leishmanial and human GDP-Mannose Pyrophosphorylases and selection of inhibitors as new leads

H. van Tilbeurgh, T. Ha-Duong, N. Lazar, 2017, Scientific Reports.

New chemical aspects of primidone metabolism

O. Lafont, C. Cavé, M. Miocque, 1990 .

Metabolic hydroxylation of amobarbital ethyl side chain

O. Lafont, C. Cavé, M. Miocque, 1985 .

Correlation between lipophilicity and reactivity under biomimetic conditions of β-hydroxybarbiturates

O. Lafont, C. Cavé, M. Miocque, 1988 .

[Stability and detection of metabolites of barbiturates: 2-oxo tetrahydro-3-furoic acids].

O. Lafont, C. Cavé, M. Miocque, 1988, Annales pharmaceutiques francaises.

ENANTIOSELECTIVE ACCESS TO FIVE- AND SIX-MEMBERED NITROGEN-CONTAINING HETEROCYCLES, BASED ON THE ASYMMETRIC MICHAEL ADDITION OF CHIRAL IMINES AND CHIR AL ENAMINO ESTERS

A. Gassama, D. Desmaële, J. D'angelo, 1998 .

Synthesis of 19β,28-epoxy-23,24-dinor-A-neo-18α-olean-4-en-3-one from betulin

C. Cavé, F. Galin, O. S. Kukovinets, 2007 .

Comparative study of structural models of Leishmania donovani and human GDP-mannose pyrophosphorylases.

T. Ha-Duong, P. Loiseau, C. Cavé, 2016, European journal of medicinal chemistry.

ASYMMETRIC SEQUENTIAL MICHAEL ADDITION-N-HETEROCYCLIZATION REACTIONS INVOLVING CHIRAL IMINES

D. Desmaële, J. D'angelo, C. Cavé, 1997 .

Asymmetric Sequential Michael Addition‐N‐Heterocyclization Reactions Involving Chiral Imines

D. Desmaële, J. D'angelo, C. Cavé, 1997 .

Asymmetric bridging annulation reaction involving the intramolecular conjugate addition of chiral imines to enoates: Access to a polycyclic system related to the taxane core

J. D'angelo, C. Cavé, F. Dumas, 1995 .

Mukaiyama-type, eight-membered ring closure: Access to a tricyclic system related to taxanes

J. D'angelo, C. Cavé, R. Casas, 1998 .

Asymmetric Bridging Annulation Reaction Involving the Intramolecular Conjugate Addition of Chiral Imines to Enoates: Access to a Polycyclic System Related to the Taxane Core.

J. D'angelo, C. Cavé, F. Dumas, 1996 .

Stereocontrolled access to α-fluoro-β-ketoesters

G. Morgant, Sandrine Delarue-Cochin, C. Cavé, 2007 .

Regio- and stereoselective aspects in the oxidation of (R) and (S) 4a-methyl-(4,4a,5,6,7,8)-hexahydro-2(3H)naphthalenones in living rats

P. Vérité, J. D'angelo, O. Lafont, 1997 .

Regio‐ and Stereoselective Aspects in the Oxidation of (R)‐ and (S)‐4a‐ Methyl‐(4,4a,5,6,7,8)‐hexahydro‐2(3H)naphthalenones in Living Rats.

P. Vérité, J. D'angelo, O. Lafont, 1997 .

In silico analysis of a therapeutic target in Leishmania infantum: the guanosine-diphospho-D-mannose pyrophosphorylase

P. Loiseau, J. Rodrigo, C. Cavé, 2012, Parasite.

In Silico Target Druggability Assessment: From Structural to Systemic Approaches.

Christian Cavé, Jean-Yves Trosset, J. Trosset, 2019, Methods in molecular biology.

In Silico Drug-Target Profiling.

Christian Cavé, Jean-Yves Trosset, J. Trosset, 2019, Methods in molecular biology.

Ortho-metalated aromatic tertiary amides: New synthetic applications

J. D'angelo, C. Cavé, R. Casas, 1995 .