about
Discovery of azaisoerianin derivatives as potential antitumors agents.Palladium-Mediated Labeling of Nucleic Acids.Heat shock proteins and cancer: How can nanomedicine be harnessed?Controllable Activation of Pd-G3 Palladacycle Precatalyst in the Presence of Thiosugars: Rapid Access to 1-Aminobiphenyl Thioglycoside Atropoisomers at Room Temperature.Stereoretentive Copper-Catalyzed Directed Thioglycosylation of C(sp2 )-H Bonds of Benzamides.Efficient Buchwald-Hartwig-Migita Cross-Coupling for DNA Thioglycoconjugation.Palladium-Catalyzed Chemoselective and Biocompatible Functionalization of Cysteine-Containing Molecules at Room Temperature.Synthesis of (1 → 2)-S-Linked Saccharides and S-Linked Glycoconjugates via a Palladium-G3-XantPhos Precatalyst Catalysis.Convergent Synthesis of N,S-bis Glycosylquinolin-2-ones via a Pd-G3-XantPhos Precatalyst Catalysis.One-Pot Assembly of Unsymmetrical Biaryl Thioglycosides through Chemoselective Palladium-Catalyzed Three-Component Tandem Reaction.Convergent Strategy to Dizocilpine MK-801 and DerivativesIntramolecular Pd-Catalyzed Anomeric C(sp3)-H Activation of Glycosyl CarboxamidesConversion of 3-Bromo-2H-coumarins to 3-(Benzofuran-2-yl)-2H-coumarins under Palladium Catalysis: Synthesis and Photophysical Properties StudyElectrochemical nickel-catalyzed Migita cross-coupling of 1-thiosugars with aryl, alkenyl and alkynyl bromidesSynthesis of aryl-thioglycopeptides through chemoselective Pd-mediated conjugationCopper-Catalyzed Anomeric O-Arylation of Carbohydrate Derivatives at Room TemperatureSynthesis of 2,3-Substituted β-N-Glycosyl Indoles through C-H Activation/Annulation Process under Rh(III)-CatalysisNi/Photoredox-Dual-Catalyzed Functionalization of 1-ThiosugarsSynthesis of N-Glycosyl-2-oxindoles by Pd-Catalyzed N-Arylation of 1-AmidosugarsRegio- and diastereoselective Pd-catalyzed synthesis of C2-aryl glycosides
P50
Q39010208-C9981D70-5FDE-452F-9BA5-40D611A5E668Q39045835-3B02C5F5-E01F-4D56-A3E7-26792C3F3031Q39088929-5A93D73F-3CC6-4EC4-BFBB-F6BC50563978Q47825750-C8EB91B5-08C9-4119-B51B-F57CC315109EQ48097463-4A017856-38F9-4105-90DA-4DDF6ECE6683Q48179363-713E9C40-908C-4776-B0C0-73514A83784FQ48180255-BDC3414C-63AA-4A16-9F3E-5026A79E9041Q48300586-2A14FE5D-D738-4598-B836-6085AF19451FQ52679126-4DBAAEEE-0C10-4E3F-90FA-977FCDBFE884Q64956601-658F0424-F15D-4FA0-89BF-A781E02EF082Q87907464-0FEEF24C-AA4D-4E00-8F94-CB6B919B5B63Q88970214-5365EB1C-1B54-418A-8D88-27D5C0695E57Q89230755-7587B1C5-001E-4865-9323-E43FED0E985FQ90495395-BC9BEE24-ED34-4D4A-8027-F28B09EC75F6Q90972807-73AA1F5B-D9B5-4B4B-A8E8-E1047B4A5710Q91630969-5499DBB6-9094-4B62-8012-CBA87728C65DQ92148326-E5F83920-7D25-432D-B43C-4D103829276EQ93079866-FE252870-F947-4902-B2E1-E79395B3BA61Q94652830-F1B3CBE9-DBC1-4F04-89D9-81D727891730Q95939392-9DBAD625-3D8B-488B-8F1B-7C587F5F87BD
P50
description
investigador
@es
researcher
@en
name
Samir Messaoudi
@en
type
label
Samir Messaoudi
@en
prefLabel
Samir Messaoudi
@en
P31
P496
0000-0002-4994-9001