N. Boutard

发表

New C-Glycosylated α-Amino Acid Synthesis by Addition Reaction of an Amino Acid Organozinc Reagent on Carbohydrate-Derived Aldehydes

Jean Martínez, J. Lavergne, F. Labéguère, 2012 .

Positional scanning for peptide secondary structure by systematic solid-phase synthesis of amino lactam peptides.

S. Chemtob, W. Lubell, H. Ong, 2009, Journal of the American Chemical Society.

Beta,beta-disubstituted C- and N-vinylindoles from one-step condensations of aldehydes and indole derivatives.

W. Lubell, G. Fridkin, N. Boutard, 2009, The Journal of organic chemistry.

β,β-Disubstituted C- and N-Vinylindoles from One-Step Condensations of Aldehydes and Indole Derivatives.

G. Fridkin, N. Boutard, Willliam D. Lubell, 2010 .

Peptide Scanning for Studying Structure‐Activity Relationships in Drug Discovery

W. Lubell, David Sabatino, A. Jamieson, 2013, Chemical biology & drug design.

Discovery and Structure–Activity Relationships of N‐Aryl 6‐Aminoquinoxalines as Potent PFKFB3 Kinase Inhibitors

M. Jurzak, M. Nowak, M. Kujawa, 2018, ChemMedChem.

Structure–Activity Analysis of the Growth Hormone Secretagogue GHRP‐6 by α‐ and β‐Amino γ‐Lactam Positional Scanning

W. Lubell, H. Ong, A. Jamieson, 2010, Chemical biology & drug design.

Pyrrolo[3,2-e][1,4]diazepin-2-one synthesis: a head-to-head comparison of soluble versus insoluble supports.

W. Lubell, Julien Dufour-Gallant, N. Boutard, 2011, The Journal of organic chemistry.

Synthetic Lethality Triggered by Combining Olaparib with BRCA2-Rad51 Disruptors.

A. Cavalli, S. Minucci, G. Di Stefano, 2017, ACS chemical biology.

5-Keto-3-cyano-2,4-diaminothiophenes as selective maternal embryonic leucine zipper kinase inhibitors.

M. Milik, M. Żurawska, Karolina Gluza, 2019, Bioorganic & medicinal chemistry letters.

Examination of the active secondary structure of the peptide 101.10, an allosteric modulator of the interleukin‐1 receptor, by positional scanning using β‐amino γ‐lactams

S. Chemtob, W. Lubell, C. Quiniou, 2011, Journal of peptide science : an official publication of the European Peptide Society.

Discovery of a Series of Ester-substituted NLRP3 Inflammasome Inhibitors.

C. Gabel, R. Porter, J. Doedens, 2020, Bioorganic & medicinal chemistry letters.

Synthesis of amide and sulfonamide substituted N-aryl 6-aminoquinoxalines as PFKFB3 inhibitors with improved physicochemical properties.

M. Jurzak, M. Nowak, M. Kujawa, 2019, Bioorganic & medicinal chemistry letters.

Discovery and Structure-Activity Relationships of N-Aryl 6-Aminoquinoxalines as Potent PFKFB3 Kinase Inhibitors.

M. Jurzak, M. Nowak, M. Kujawa, 2018 .

Human PFKFB3 in complex with a N-Aryl 6-Aminoquinoxaline inhibitor 4

M. Nowak, M. Mikulski, H. Eggenweiler, 2019 .