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Recent Advances in Transition-Metal-Free Late-Stage C-H and N-H Arylation of Heteroarenes Using Diaryliodonium Salts

Pharmaceuticals (Basel, Switzerland), 2021-07, Vol.14 (7), p.661

2021

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Synthesis of 2-Cyanobenzothiazoles via Pd-Catalyzed/Cu-Assisted C-H Functionalization/Intramolecular C-S Bond Formation from N -Arylcyanothioformamides

Molecules (Basel, Switzerland), 2022-12, Vol.27 (23), p.8426

2022

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Microwave-Assisted Sequential One-Pot Synthesis of 8-Substituted Pyrazolo[1,5-a][1,3,5]triazines

Molecules (Basel, Switzerland), 2021-06, Vol.26 (12), p.3540

2021

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Review on the Synthesis and Therapeutic Potential of Pyrido[2,3- d ], [3,2- d ], [3,4- d ] and [4,3- d ]pyrimidine Derivatives

Pharmaceuticals (Basel, Switzerland), 2022-03, Vol.15 (3), p.352

2022

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Diaryliodoniums Salts as Coupling Partners for Transition-Metal Catalyzed C- and N-Arylation of Heteroarenes

Catalysts, 2020-05, Vol.10 (5), p.483

2020

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A novel DYRK1A (Dual specificity tyrosine phosphorylation‐regulated kinase 1A) inhibitor for the treatment of Alzheimer's disease: effect on Tau and amyloid pathologies in vitro

Journal of neurochemistry, 2015-05, Vol.133 (3), p.440-451

2015

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Demonstration of Green Solvent Performance on O,S,N-Heterocycles Synthesis: Metal-Free Click Chemistry and Buchwald-Hartwig Coupling

Molecules (Basel, Switzerland), 2021-02, Vol.26 (4), p.1074

2021

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Straightforward Access to a New Class of Dual DYRK1A/CLK1 Inhibitors Possessing a Simple Dihydroquinoline Core

Molecules (Basel, Switzerland), 2023-01, Vol.28 (1), p.36

2023

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Relieving DYRK1A repression of MKL1 confers an adult-like phenotype to human infantile megakaryocytes

The Journal of clinical investigation, 2022-10, Vol.132 (19)

2022

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DYRK1A controls the transition from proliferation to quiescence during lymphoid development by destabilizing Cyclin D3

The Journal of experimental medicine, 2015-06, Vol.212 (6), p.953-970

2015

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26th Annual GP2A Medicinal Chemistry Conference & 32nd Journées Franco-Belges de Pharmacochimie

Pharmaceuticals (Basel, Switzerland), 2019-05, Vol.12 (2), p.73

2019

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Design and synthesis of thiazolo[5,4-f]quinazolines as DYRK1A inhibitors, part II

Molecules (Basel, Switzerland), 2014-09, Vol.19 (10), p.15411-15439

2014

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Copper-Catalyzed C–H Arylation of Fused-Pyrimidinone Derivatives Using Diaryliodonium Salts

Catalysts, 2021-01, Vol.11 (1), p.28

2021

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Microwave-Assisted Synthesis of Potential Bioactive Benzo-, Pyrido- or Pyrazino-thieno[3,2-d]pyrimidin-4-amine Analogs of MPC-6827

Pharmaceuticals (Basel, Switzerland), 2020-09, Vol.13 (9), p.202

2020

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Design and synthesis of thiazolo[5,4-f]quinazolines as DYRK1A inhibitors, part I

Molecules (Basel, Switzerland), 2014-09, Vol.19 (10), p.15546-15571

2014

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Exploring Kinase Inhibition Properties of 9H-pyrimido[5,4-b]- and [4,5-b]indol-4-amine Derivatives

Pharmaceuticals (Basel, Switzerland), 2020-05, Vol.13 (5), p.89

2020

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Synthesis of Thiazolo[5,4-f]quinazolin-9(8H)-ones as Multi-Target Directed Ligands of Ser/Thr Kinases

Molecules (Basel, Switzerland), 2016-04, Vol.21 (5), p.578

2016

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The Chromosome 21 Kinase DYRK1A and Its Substrate FOXO1 Constitute a Novel Therapeutic Pathway in B-ALL

Blood, 2018-11, Vol.132 (Supplement 1), p.548-548

2018

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Development of Kinase Inhibitors via Metal-Catalyzed C⁻H Arylation of 8-Alkyl-thiazolo[5,4- f ]-quinazolin-9-ones Designed by Fragment-Growing Studies

Molecules (Basel, Switzerland), 2018-08, Vol.23 (9), p.2181

2018

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Synthesis of 2-Mercapto-(2-Oxoindolin-3-Ylidene)Acetonitriles from 3-(4-Chloro-5 H -1,2,3-Dithiazol-5-Ylidene)Indolin-2-ones

Molecules (Basel, Switzerland), 2018-06, Vol.23 (6), p.1390

2018

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Synthesis of Bioactive 2-(Arylamino)thiazolo[5,4-f]-quinazolin-9-ones via the Hügershoff Reaction or Cu- Catalyzed Intramolecular C-S Bond Formation

Molecules (Basel, Switzerland), 2016-06, Vol.21 (6), p.794

2016

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Microwave-assisted synthesis of bioactive quinazolines and quinazolinones

Combinatorial chemistry & high throughput screening, 2007-12, Vol.10 (10), p.903-917

2007

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Recent Developments in Microwave-Assisted Metal-Catalyzed C–H Functionalization of Heteroarenes for Medicinal Chemistry and Material Applications

Synthesis (Stuttgart), 2016-11, Vol.48 (22), p.3879-3889

2016

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Microwave acceleration of the Pechmann reaction on graphite/montmorillonite K10: application to the preparation of 4-substituted 7-aminocoumarins

Tetrahedron letters, 2001-04, Vol.42 (15), p.2791-2794

2001

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Recent Advances in Transition-Metal-Free Late-Stage C-H and N-H Arylation of Heteroarenes Using Diaryliodonium Salts

Synthesis of 2-Cyanobenzothiazoles via Pd-Catalyzed/Cu-Assisted C-H Functionalization/Intramolecular C-S Bond Formation from N -Arylcyanothioformamides

Microwave-Assisted Sequential One-Pot Synthesis of 8-Substituted Pyrazolo[1,5-a][1,3,5]triazines

Review on the Synthesis and Therapeutic Potential of Pyrido[2,3- d ], [3,2- d ], [3,4- d ] and [4,3- d ]pyrimidine Derivatives

Diaryliodoniums Salts as Coupling Partners for Transition-Metal Catalyzed C- and N-Arylation of Heteroarenes

A novel DYRK1A (Dual specificity tyrosine phosphorylation‐regulated kinase 1A) inhibitor for the treatment of Alzheimer's disease: effect on Tau and amyloid pathologies in vitro

Demonstration of Green Solvent Performance on O,S,N-Heterocycles Synthesis: Metal-Free Click Chemistry and Buchwald-Hartwig Coupling

Straightforward Access to a New Class of Dual DYRK1A/CLK1 Inhibitors Possessing a Simple Dihydroquinoline Core

Relieving DYRK1A repression of MKL1 confers an adult-like phenotype to human infantile megakaryocytes

Efficacy of DYRK1A inhibitors in novel models of Down syndrome acute lymphoblastic leukemia

DYRK1A controls the transition from proliferation to quiescence during lymphoid development by destabilizing Cyclin D3

26th Annual GP2A Medicinal Chemistry Conference & 32nd Journées Franco-Belges de Pharmacochimie

Design and synthesis of thiazolo[5,4-f]quinazolines as DYRK1A inhibitors, part II

Copper-Catalyzed C–H Arylation of Fused-Pyrimidinone Derivatives Using Diaryliodonium Salts

Microwave-Assisted Synthesis of Potential Bioactive Benzo-, Pyrido- or Pyrazino-thieno[3,2-d]pyrimidin-4-amine Analogs of MPC-6827

Design and synthesis of thiazolo[5,4-f]quinazolines as DYRK1A inhibitors, part I

Exploring Kinase Inhibition Properties of 9H-pyrimido[5,4-b]- and [4,5-b]indol-4-amine Derivatives

Synthesis of Thiazolo[5,4-f]quinazolin-9(8H)-ones as Multi-Target Directed Ligands of Ser/Thr Kinases

The Chromosome 21 Kinase DYRK1A and Its Substrate FOXO1 Constitute a Novel Therapeutic Pathway in B-ALL

Development of Kinase Inhibitors via Metal-Catalyzed C⁻H Arylation of 8-Alkyl-thiazolo[5,4- f ]-quinazolin-9-ones Designed by Fragment-Growing Studies

Synthesis of 2-Mercapto-(2-Oxoindolin-3-Ylidene)Acetonitriles from 3-(4-Chloro-5 H -1,2,3-Dithiazol-5-Ylidene)Indolin-2-ones

Synthesis of Bioactive 2-(Arylamino)thiazolo[5,4-f]-quinazolin-9-ones via the Hügershoff Reaction or Cu- Catalyzed Intramolecular C-S Bond Formation

Microwave-assisted synthesis of bioactive quinazolines and quinazolinones

Recent Developments in Microwave-Assisted Metal-Catalyzed C–H Functionalization of Heteroarenes for Medicinal Chemistry and Material Applications

Microwave acceleration of the Pechmann reaction on graphite/montmorillonite K10: application to the preparation of 4-substituted 7-aminocoumarins

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