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New N-ribosides and N-mannosides of rhodanine derivatives with anticancer activity on leukemia cell line: Design, synthesis, DFT and molecular modelling studies

Carbohydrate research, 2020-01, Vol.487, p.107894, Article 107894

2020

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A new synthesis of trifluorinated compounds via 1,1-dichloro-1-alkenes in superacid

Tetrahedron letters, 2007-07, Vol.48 (30), p.5255-5260

2007

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A new approach for the N- and S-galactosylation of 5-arylidene-2-thioxo-4-thiazolidinones

Carbohydrate research, 2011-12, Vol.346 (18), p.2831-2837

2011

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Synthesis and Modeling of New Benzofuranone Histone Deacetylase Inhibitors that Stimulate Tumor Suppressor Gene Expression

Journal of medicinal chemistry, 2009-05, Vol.52 (9), p.3112-3115

2009

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First O-Glycosylation of Hydroxamic Acids

Journal of organic chemistry, 2007-05, Vol.72 (11), p.4262-4264

2007

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Synthesis and Conformational Analysis of Macrocycles Related to 10-Oxa-epothilone

European journal of organic chemistry, 2004-12, Vol.2004 (23), p.4762-4770

2004

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Synthesis and biological evaluation of glucuronide prodrugs of the histone deacetylase inhibitor CI-994 for application in selective cancer chemotherapy

Bioorganic & medicinal chemistry, 2008-09, Vol.16 (17), p.8109-8116

2008

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Synthetic studies on a phenyl-laulimalide analogue

Tetrahedron letters, 2006-11, Vol.47 (47), p.8305-8308

2006

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Elucidation of the mechanism enabling tumor selective prodrug monotherapy

Cancer research (Chicago, Ill.), 1998-03, Vol.58 (6), p.1195-1201

1998

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New strategy for the synthesis of phosphatase inhibitors TMC-69-6H and analogs

Tetrahedron letters, 2006-12, Vol.47 (52), p.9305-9308

2006

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gem-Difluorination of Aminoalkynes via Highly Reactive Dicationic Species in Superacid HF−SbF5: Application to the Efficient Synthesis of Difluorinated Cinchona Alkaloid Derivatives

Journal of organic chemistry, 2008-04, Vol.73 (7), p.2875-2878

2008

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An ambitious 5-year honors program in French universities: CMI-FIGURE

Journal of the European Honors Council, 2018-04, Vol.2 (1), p.1-9

2018

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Design, synthesis and biological evaluation of 1,4-benzodiazepine-2,5-dione-based HDAC inhibitors

Bioorganic & medicinal chemistry letters, 2007-09, Vol.17 (17), p.4819-4823

2007

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Synthesis and biological evaluation of the suberoylanilide hydroxamic acid (SAHA) β-glucuronide and β-galactoside for application in selective prodrug chemotherapy

Bioorganic & medicinal chemistry letters, 2007-02, Vol.17 (4), p.983-986

2007

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Synthesis of rigid trichostatin A analogs as HDAC inhibitors

Bioorganic & medicinal chemistry letters, 2006-10, Vol.16 (20), p.5339-5344

2006

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Ring closing metathesis and cross metathesis of carbohydrate derivatives

Tetrahedron letters, 1998-06, Vol.39 (23), p.4043-4046

1998

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Antiproliferative activities of a library of hybrids between indanones and HDAC inhibitor SAHA and MS-275 analogues

Bioorganic & medicinal chemistry, 2007-11, Vol.17 (22), p.6142-6146

2007

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A new simple and convenient method for the synthesis of substituted 2,6,9-trioxabicyclo[3.3.1]-nona-3,7-dienes from arylmalondialdehydes

Tetrahedron letters, 2006-08, Vol.47 (33), p.5961-5964

2006

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Biological activities of substituted trichostatic acid derivatives

Journal of chemical sciences (Bangalore, India), 2009, Vol.121 (4), p.471-479

2009

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Total Synthesis and Conformational Analysis of the Antifungal Agent (−)-PF1163B

Organic letters, 2003-10, Vol.5 (22), p.4049-4052

2003

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Click Chemistry with O-Dimethylpropargylcarbamate for Preparation of pH-Sensitive Functional Groups. A Case Study

Journal of organic chemistry, 2007-04, Vol.72 (9), p.3596-3599

2007

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New synthesis of trifluorinated amines from 1-bromopropargylic amines in superacid

Tetrahedron letters, 2006-07, Vol.47 (31), p.5547-5551

2006

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Synthesis of quinone and xanthone analogs of rhein

Tetrahedron, 2001-10, Vol.57 (44), p.9131-9135

2001

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Selective cross-metathesis of 2-allylphenols with styrenes

Tetrahedron letters, 2001-10, Vol.42 (41), p.7229-7231

2001

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SULFUR GLYCOSYLATION REACTIONS INVOLVING 3-ALLYL-2-THIOHYDANTOIN NUCLEOSIDE BASES AS POTENTIAL ANTIVIRAL AND ANTITUMOR AGENTS

Phosphorus, sulfur, and silicon and the related elements, 1998-11, Vol.142 (1), p.167-190

1998

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New N-ribosides and N-mannosides of rhodanine derivatives with anticancer activity on leukemia cell line: Design, synthesis, DFT and molecular modelling studies

A new synthesis of trifluorinated compounds via 1,1-dichloro-1-alkenes in superacid

A new approach for the N- and S-galactosylation of 5-arylidene-2-thioxo-4-thiazolidinones

Synthesis and Modeling of New Benzofuranone Histone Deacetylase Inhibitors that Stimulate Tumor Suppressor Gene Expression

First O-Glycosylation of Hydroxamic Acids

Synthesis and Conformational Analysis of Macrocycles Related to 10-Oxa-epothilone

Synthesis and biological evaluation of glucuronide prodrugs of the histone deacetylase inhibitor CI-994 for application in selective cancer chemotherapy

Synthetic studies on a phenyl-laulimalide analogue

Elucidation of the mechanism enabling tumor selective prodrug monotherapy

New strategy for the synthesis of phosphatase inhibitors TMC-69-6H and analogs

gem-Difluorination of Aminoalkynes via Highly Reactive Dicationic Species in Superacid HF−SbF5: Application to the Efficient Synthesis of Difluorinated Cinchona Alkaloid Derivatives

An ambitious 5-year honors program in French universities: CMI-FIGURE

Design, synthesis and biological evaluation of 1,4-benzodiazepine-2,5-dione-based HDAC inhibitors

Synthesis and biological evaluation of the suberoylanilide hydroxamic acid (SAHA) β-glucuronide and β-galactoside for application in selective prodrug chemotherapy

Synthesis of rigid trichostatin A analogs as HDAC inhibitors

Ring closing metathesis and cross metathesis of carbohydrate derivatives

Antiproliferative activities of a library of hybrids between indanones and HDAC inhibitor SAHA and MS-275 analogues

A new simple and convenient method for the synthesis of substituted 2,6,9-trioxabicyclo[3.3.1]-nona-3,7-dienes from arylmalondialdehydes

Biological activities of substituted trichostatic acid derivatives

Total Synthesis and Conformational Analysis of the Antifungal Agent (−)-PF1163B

Click Chemistry with O-Dimethylpropargylcarbamate for Preparation of pH-Sensitive Functional Groups. A Case Study

New synthesis of trifluorinated amines from 1-bromopropargylic amines in superacid

Synthesis of quinone and xanthone analogs of rhein

Selective cross-metathesis of 2-allylphenols with styrenes

SULFUR GLYCOSYLATION REACTIONS INVOLVING 3-ALLYL-2-THIOHYDANTOIN NUCLEOSIDE BASES AS POTENTIAL ANTIVIRAL AND ANTITUMOR AGENTS

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