A. Tikad

发表

1,4-Dioxins, Oxathiins, Dithiins and Their Benzo Derivatives

S. El Kazzouli, G. Guillaumet, A. Tikad, 2020, Reference Module in Chemistry, Molecular Sciences and Chemical Engineering.

Identification of a cytotoxic molecule in heat-modified citrus pectin.

C. Michiels, M. Dieu, P. Cambier, 2016, Carbohydrate polymers.

Synthesis of a novel UDP-carbasugar as UDP-galactopyranose mutase inhibitor.

Sandy El Bkassiny, C. M. Sevrain, A. Tikad, 2014, Organic letters.

Synthesis of Unprecedented Sulfonylated Phosphono-exo-Glycals Designed as Inhibitors of the Three Mycobacterial Galactofuranose Processing Enzymes.

T. Lowary, W. Pan, R. Zheng, 2016, Chemistry.

Selectfluor and NFSI exo-glycal fluorination strategies applied to the enhancement of the binding affinity of galactofuranosyltransferase GlfT2 inhibitors.

G. Besra, G. Eppe, A. Ardá, 2014, Chemistry.

β-Stereoselective phosphorylations applied to the synthesis of ADP- and polyprenyl-β-mannopyranosides.

W. Pan, Tianlei Li, A. Tikad, 2014, Organic letters.

Efficient microwave-assisted Suzuki–Miyaura cross-coupling reaction of 3-bromo pyrazolo[1,5-a]pyrimidin-5(4H)-one: towards a new access to 3,5-diarylated 7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine derivatives

M. Akssira, G. Guillaumet, M. Abarbri, 2021, RSC advances.

Suzuki Coupling Reactions of (E)- and (Z)-Chloroenynes with Boronic Acids: Versatile Access to Functionalized 1,3-Enynes

J. Brion, M. Alami, Abdallah Hamze, 2010 .

β-Selective one-pot fluorophosphorylation of d,d -heptosylglycals mediated by selectfluor

A. Tikad, S. Vincent, 2015 .

Systematic synthesis of inhibitors of the two first enzymes of the bacterial heptose biosynthetic pathway: towards antivirulence molecules targeting lipopolysaccharide biosynthesis.

M. Durka, F. Moreau, V. Gerusz, 2011, Chemistry.

A General Strategy to Synthesize ADP-7-Azido-heptose and ADP-Azido-mannoses and Their Heptosyltransferase Binding Properties.

E. Taylor, W. Pan, Tianlei Li, 2021, Organic letters.

Mechanistic Insight into Heptosyltransferase Inhibition by using Kdo Multivalent Glycoclusters.

S. Laurent, J. Nierengarten, C. M. Sevrain, 2016, Chemistry.

Multigram-scale synthesis of l,d-heptoside using a Fleming-Tamao oxidation promoted by mercuric trifluoroacetate.

W. Pan, M. Durka, Tianlei Li, 2016, Carbohydrate research.

Stereocontrolled β- and α-Phosphorylations of d-Mannose

W. Pan, Y. Brissonnet, Tianlei Li, 2015 .

Constrained 3,6-Anhydro-Heptosides: Synthesis by a DAST-Induced Debenzylative Reaction, and Reactivity Profile

A. Tikad, S. Vincent, 2013 .

Synthetic Methodologies toward Aldoheptoses and Their Applications to the Synthesis of Biochemical Probes and LPS Fragments

A. Tikad, S. Vincent, 2013 .

Regioselective Synthesis of Difluorinated C-Furanosides Involving a Debenzylative Cycloetherification.

A. Tikad, S. Vincent, J. Delbrouck, 2019, Organic letters.

New efficient route to dissymmetric 2,4-di(het)aryl-pyrido[3,2-d]pyrimidines via regioselective cross-coupling reactions.

J. Leger, C. Jarry, M. Akssira, 2007, Organic Letters.

Highly ( Z)-Diastereoselective Synthesis of Trifluoromethylated exo-Glycals via Photoredox and Copper Catalysis.

J. Cornil, R. Robiette, Lidia Dumitrescu, 2018, Organic letters.

Regiocontroled SNAr and Palladium Cross‐Coupling Reactions of 2,4,7‐Trichloropyrido[3,2‐d]pyrimidine

J. Leger, C. Jarry, M. Akssira, 2012 .

Efficient hydration of nitriles to amides catalysed by sodium nitrate modified fluorapatite

D. Macquarrie, S. Sebti, A. Solhy, 2003 .

Potassium fluoride doped fluorapatite and hydroxyapatite as new catalysts in organic synthesis

S. Sebti, A. Solhy, A. Tikad, 2003 .

Efficient one-pot synthesis of 2,4-di(het)aryl and 2,4-diamino pyrido[3,2-d]pyrimidines involving regioselective S(N)Ar and palladium-catalyzed reactions.

M. Akssira, S. Routier, G. Guillaumet, 2009, Organic & biomolecular chemistry.

Debenzylative Cycloetherification: An Overlooked Key Strategy for Complex Tetrahydrofuran Synthesis.

A. Tikad, S. Vincent, J. Delbrouck, 2016, Chemistry.

Efficient Access to 3,5-Disubstituted 7-(Trifluoromethyl)pyrazolo[1,5-a]pyrimidines Involving SNAr and Suzuki Cross-Coupling Reactions

M. Akssira, G. Guillaumet, M. Abarbri, 2020, Molecules.

Efficient and regioselective synthesis of γ-lactone glycosides through a novel debenzylative cyclization reaction.

A. Tikad, S. Vincent, J. Delbrouck, 2018, Chemical communications.

Efficient Synthesis of tert ‐Butyl 2,4‐Dialkynylated and 2‐Alkynylated‐4‐Arylated‐1 H ‐Imidazole‐1‐Carboxylate via Regioselective Sonogashira Cross‐Coupling Reaction

A. E. Qami, J. Jacquemin, R. Guillot, 2021, European Journal of Organic Chemistry.

A new strategy for selective targeting of progesterone receptor with passive antagonists.

M. Lombès, N. Chabbert-Buffet, G. Meduri, 2013, Molecular endocrinology.

Synthesis and optimization of an original V-shaped collection of 4-7-disubstituted pyrido[3,2-d]pyrimidines as CDK5 and DYRK1A inhibitors.

L. Meijer, P. Bonnet, O. Lozach, 2014, European journal of medicinal chemistry.

Efficient Synthesis of 1H-Benzo[4,5]imidazo[1,2-c][1,3]oxazin-1-one Derivatives Using Ag2CO3/TFA-Catalyzed 6-endo-dig Cyclization: Reaction Scope and Mechanistic Study

J. Jacquemin, M. Akssira, M. Abarbri, 2023, Molecules.

MPHT-Promoted Bromocyclization of ortho-Substituted Arylalkynes: Application to the Synthesis of 2-Substituted 3-Bromobenzofurans and -Benzo[b]thiophenes

J. Brion, M. Alami, Abdallah Hamze, 2010 .

Synthesis and optimization of an original V-shaped collection of 4-7-disubstituted pyrido[3,2-d]pyrimidines as CDK5 and DYRK1A inhibitors.

L. Meijer, P. Bonnet, O. Lozach, 2014, European journal of medicinal chemistry.