C. Montalbetti

发表

Amide bond formation and peptide coupling

C. Montalbetti, Virginie M. Falque, Christian A.G.N. Montalbetti, 2005 .

Investigation of a New Family of Chiral Ligands for Enantioselective Catalysis via Parallel Synthesis and High-Throughput Screening

S. Ceccarelli, R. F. Jackson, C. Montalbetti, 1998 .

Synthetic strategies to prepare 2-alkyl, 2-aryl and 2-acetylenyl substituted 4,6-diamino-1,3,5-triazines

M. K. Uddin, C. Krog-Jensen, J. Felding, 2006 .

Structure-based design and synthesis of potent benzothiazole inhibitors of interleukin-2 inducible T cell kinase (ITK).

Adam R. Johnson, S. Bromidge, Lawren C. Wu, 2013, Bioorganic & medicinal chemistry letters.

Synthetic Chemistry: Formation of the Amide Bond

C. Montalbetti, Virginie M. Falque, 2008 .

Chiral Resolution and Pharmacological Characterization of the Enantiomers of the Hsp90 Inhibitor 2‐Amino‐7‐[4‐fluoro‐2‐(3‐pyridyl)phenyl]‐4‐methyl‐7,8‐dihydro‐6H‐quinazolin‐5‐one Oxime

S. Minucci, C. Mercurio, R. Amici, 2014, ChemMedChem.

Synthetic Chemistry: Formation of the Amide Bond

C. Montalbetti, Virginie M. Falque, 2008 .

Design, Synthesis, and Evaluation of a Novel Series of Indole Sulfonamide Peroxisome Proliferator Activated Receptor (PPAR) α/γ/δ Triple Activators: Discovery of Lanifibranor, a New Antifibrotic Clinical Candidate.

J. Binet, J. Junien, Stéphanie Ferry, 2018, Journal of medicinal chemistry.

C–H Halogenation of Pyridyl Sulfides Avoiding the Sulfur Oxidation: A Direct Catalytic Access to Sulfanyl Polyhalides and Polyaromatics

N. Pirio, Jean‐Cyrille Hierso, C. Montalbetti, 2019, ACS omega.

Existence of a Preferred Orientation for the Methoxy Group on an Extended Aromatic System.

C. Montalbetti, I. Braccini, J. Amaudrut, 2018, ChemistrySelect.

Syntheses and antiproliferative evaluation of oxyphenisatin derivatives.

M. K. Uddin, C. Krog-Jensen, Steven Butcher, 2007, Bioorganic & medicinal chemistry letters.

Structure-Based Design of Tricyclic NF-κB Inducing Kinase (NIK) Inhibitors That Have High Selectivity over Phosphoinositide-3-kinase (PI3K).

Adam R. Johnson, Jianwen A. Feng, Brandon J. Bravo, 2017, Journal of medicinal chemistry.

(2‐Pyridyl)sulfonyl Groups for ortho‐Directing Palladium‐ Catalyzed Carbon–Halogen Bond Formation at Functionalized Arenes

H. Cattey, N. Pirio, Jean‐Cyrille Hierso, 2017 .

Conformational analysis of (R,S)-4-amido-2,4-dimethyl-butyric acid derivatives

R. W. Hoffmann, E. Framery, F. Caturla, 1999 .

A convergent synthesis of functionalized B-seco taxane skeletons

M. Savignac, J. Genêt, C. Montalbetti, 1995 .

Remote substituent control of the regioselectivity of the aryl- and vinylpalladation of 7-oxabicyclo[2.2.1]heptenes

P. Vogel, M. Savignac, J. Genêt, 1996 .

Direct synthesis of Fmoc-protected amino acids using organozinc chemistry: application to polymethoxylated phenylalanines and 4-oxoamino acids

C. Montalbetti, H. Deboves, R. Jackson, 2001 .

Azide-free synthesis of Boc-protected (3R,4S)-3,4-dihydroxypiperidine

A. Petrocchi, F. Ferrigno, Nicola Relitti, 2022, Tetrahedron Letters.

The synthesis and evaluation of indolylureas as PKCα inhibitors.

Andrew N. Carr, A. Gołębiowski, C. Montalbetti, 2011, Bioorganic & medicinal chemistry.

Fragment‐based Identification of Hsp90 Inhibitors

Mark Whittaker, Thomas Hesterkamp, Dirk Winkler, 2009, ChemMedChem.

Design, synthesis and structure-activity relationships of a novel class of sulfonylpyridine inhibitors of Interleukin-2 inducible T-cell kinase (ITK).

Adam R. Johnson, P. McEwan, A. Zarrin, 2014, Bioorganic & medicinal chemistry letters.

Discovery and structure-activity relationships of novel selective norepinephrine and dual serotonin/norepinephrine reuptake inhibitors.

J. Findlay, P. Gallagher, J. Boot, 2005, Bioorganic & medicinal chemistry letters.

HCV NS5B polymerase inhibitors 2: Synthesis and in vitro activity of (1,1-dioxo-2H-[1,2,4]benzothiadiazin-3-yl) azolo[1,5-a]pyridine and azolo[1,5-a]pyrimidine derivatives.

R. Cheng, K. Kossen, S. Seiwert, 2009, Bioorganic & medicinal chemistry letters.

Discovery of a Novel Hsp90 Inhibitor by Fragment Linking

Mark Whittaker, Thomas Hesterkamp, Oliver Barker, 2010, ChemMedChem.

Discovery of novel quinoline sulphonamide derivatives as potent, selective and orally active RORγ inverse agonists.

S. Gauld, K. Cusack, M. Kort, 2019, Bioorganic & medicinal chemistry letters.