about
Aromatic tripodal receptors for (C(60)-I(h))[5,6]fullerene.Enantioselective reduction of ketoimines promoted by easily available (S)-proline derivatives.HSiCl3-Mediated Reduction of Nitro-Derivatives to Amines: Is Tertiary Amine-Stabilized SiCl2 the Actual Reducing Species?The intramolecular interaction of thiophene and furan with aromatic and fluoroaromatic systems in some [3.3]meta(heterocyclo)paracyclophanes: a combined computational and NMR spectroscopic study.Poly(ethylene glycol)-supported bisoxazolines as ligands for catalytic enantioselective synthesis.Efficient and highly stereoselective synthesis of a beta-lactam inhibitor of the serine protease prostate-specific antigen.Efficient synthesis of an enantiopure beta-lactam as an advanced precursor of thrombin and tryptase inhibitors.Chiral hybrid inorganic-organic materials: synthesis, characterization, and application in stereoselective organocatalytic cycloadditions.Stereoselective metal-free catalytic synthesis of chiral trifluoromethyl aryl and alkyl amines.Enantioselective catalysis in water: Mukaiyama-aldol condensation promoted by copper complexes of bisoxazolines supported on poly(ethylene glycol).Stereoselective synthesis and characterization of new enantiomerically pure phosphoric acids.Through-space interactions between parallel-offset arenes at the van der Waals distance: 1,8-diarylbiphenylene syntheses, structure and QM computations.The intramolecular edge-to-face interactions of an aryl C-H bond and of a pyridine nitrogen lone-pair with aromatic and fluoroaromatic systems in some [3,3]metaparacyclophanes: a combined computational and NMR study.Enantioselective catalytic reduction of ketoimines with trichlorosilane promoted by readily available chiral Lewis bases.Readily available pyridine- and quinoline-N-oxides as new organocatalysts for the enantioselective allylation of aromatic aldehydes with allyl(trichloro)silane.Steric and electronic tuning of chiral bis(oxazoline) ligands with 3,3'-bithiophene backbone.Enantioselective organocatalytic reduction of β-trifluoromethyl nitroalkenes: an efficient strategy for the synthesis of chiral β-trifluoromethyl amines.Structurally simple pyridine N-oxides as efficient organocatalysts for the enantioselective allylation of aromatic aldehydes.Very mild, enantioselective synthesis of propargylamines catalyzed by copper(I)-bisimine complexes.X-ray diffraction and theoretical studies for the quantitative assessment of intermolecular arene-perfluoroarene stacking interactions.Through-space interactions between face-to-face, center-to-edge oriented arenes: importance of polar-pi effects.Iron catalyzed diastereoselective hydrogenation of chiral imines.Stereoselective Catalytic Synthesis of Active Pharmaceutical Ingredients in Homemade 3D-Printed Mesoreactors.Stereoselective reaction of 2-carboxythioesters-1,3-dithiane with nitroalkenes: an organocatalytic strategy for the asymmetric addition of a glyoxylate anion equivalent.Stereoselective Reduction of Imines with Trichlorosilane Using Solid-Supported Chiral Picolinamides.Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensationContinuous-Flow Stereoselective Synthesis in Microreactors: Nucleophilic Additions to Nitrostyrenes Organocatalyzed by a Chiral Bifunctional CatalystStereoselective Metal-Free Reduction of Chiral Imines in Batch and Flow Mode: A Convenient Strategy for the Synthesis of Chiral Active Pharmaceutical IngredientsSynthesis of an advanced precursor of Rivastigmine: Cinchona -derived quaternary ammonium salts as organocatalysts for stereoselective imine reductionsSynthesis of novel cinchona-amino acid hybrid organocatalysts for asymmetric catalysisCinchona-Derived Picolinamides: Effective Organocatalysts for Stereoselective Imine HydrosilylationSynthesis in mesoreactors: Ru(porphyrin)CO-catalyzed aziridination of olefins under continuous flow conditionsA chiral organocatalytic polymer-based monolithic reactorSynthesis of oligopyridines and their metal complexes as precursors to topological stereoisomersSynthesis of poly(ethylene glycol)-supported manganese porphyrins: efficient, recoverable and recyclable catalysts for epoxidation of alkenesPolymer-supported organic catalystsA poly(ethylene glycol)-supported quaternary ammonium salt: An efficient, recoverable, and recyclable phase-transfer catalystPoly(ethylene glycol)-supported TEMPO: an efficient, recoverable metal-free catalyst for the selective oxidation of alcoholsStereoselective synthesis of new beta-lactams by cyclocondensation of 1-methoxy-3-(trimethylsilyloxy)-1,3-butadiene with 4-formyl substituted azetidinonesPoly(ethylene glycol)-supported tetrahydroxyphenyl porphyrin: a convenient, recyclable catalyst for photooxidation reactions
P50
Q33496807-81838D39-0CBA-4BFB-BDB7-719C642E56AEQ34686772-8E5CF51F-DF5C-4779-8F48-6C7DDD2B316DQ39951551-D4F3B38A-94FA-46D2-9D6C-BBDAA34C437AQ43011680-1756426E-1AC8-4E1C-9B17-5253E1191D4CQ43590093-D9B8A36A-226B-4AA5-979A-8A80E9CFD7D4Q43950530-1825C53A-E28E-48AE-A7C6-80704326ED2AQ44380276-344F6220-DE60-4D04-86D0-D3461D300EF9Q44893285-4B011E59-9740-4C8E-A838-8949783D724FQ45026046-E2BD3868-55E0-402E-8024-9350C6867AB9Q45144942-1EB7FBAC-0891-44E2-AA2D-2DE3C6071D76Q45935821-18D77B00-540C-402F-A90B-77F6AE315F0DQ45984504-5FC8BC9C-235F-40D2-845D-6EC1DEC73A97Q46091245-FC0E9739-BCD2-46EC-BB55-9C3D685C6D04Q46360686-E1FB6836-F1DC-4079-AF48-B4FA7A0340A8Q46577986-08E8A563-90FD-4053-A6A9-63DE0AE114B1Q46692559-320EC893-8305-46BE-B80E-45DF5C7E923DQ46788808-F76D32B3-6C41-4066-AB31-0D25D308C9A3Q46936363-8CA78D73-D7FF-4245-8251-C52D99435B8EQ46959555-B894F8F6-FCF8-4AB4-8970-B072D9D7ECF4Q46967273-8D9DCB5F-74F2-4AD4-BD93-51474E78CEF6Q47676463-59B9A10A-4D1F-436F-B131-AF82727F0DCDQ48203531-AB7B6277-3671-45CE-B45B-B2C332698289Q48360525-6C15D28E-825A-4A06-A8B6-0B8851DA3C38Q50988101-01FFE544-7484-481F-B5E4-890937146CAFQ51818462-198816D2-F539-4C73-8292-0457F9CE0D03Q56995205-564FFF65-1B73-4297-ACE3-4C1949E81448Q58560826-F14FA347-50D7-4D58-9268-54590E58EDBCQ58841859-95179E3C-664C-4A61-B5CB-16256D14DCA0Q58841884-2635916F-64DF-41B0-9CCA-4FC8B9EC6A5FQ58841887-B00BFAF6-F51D-4010-B4C4-EDC48F2BC67CQ58841891-B18721DF-F181-4F29-BADE-5ECD0F1124C4Q59078931-502B5E8E-50DE-4700-9BBE-5228285C5A62Q60166096-E33E99E7-57D4-44F0-A449-63796C8D333CQ73691733-F4EB94D9-7F09-45A3-B7BB-326FBBF67799Q73823689-D61B5391-F51E-440B-AE8B-A7716C25883FQ73921873-54BCDA37-83AE-47ED-8FE3-F30A843B36C3Q73953910-6DD51B02-B28F-4BE3-8142-AF12D378F5ECQ75351643-264009F1-BB90-4309-88F0-C9E9B8E3794EQ77332562-BBFD749A-CF25-4997-AB9B-0DD614D74CE1Q78547667-75204466-DB2F-4612-8B17-1537E0AA3108
P50
description
Itaalia keemik
@et
Italian chemist
@en
Italian chemist
@en-ca
Italian chemist
@en-gb
chimico italiano
@it
chimist italian
@ro
chimiste italien
@fr
kimist italian
@sq
químic italià
@ca
químico italiano
@es
name
Maurizio Benaglia
@ast
Maurizio Benaglia
@de
Maurizio Benaglia
@en
Maurizio Benaglia
@eo
Maurizio Benaglia
@es
Maurizio Benaglia
@fr
Maurizio Benaglia
@it
Maurizio Benaglia
@la
Maurizio Benaglia
@nl
Maurizio Benaglia
@pt
type
label
Maurizio Benaglia
@ast
Maurizio Benaglia
@de
Maurizio Benaglia
@en
Maurizio Benaglia
@eo
Maurizio Benaglia
@es
Maurizio Benaglia
@fr
Maurizio Benaglia
@it
Maurizio Benaglia
@la
Maurizio Benaglia
@nl
Maurizio Benaglia
@pt
prefLabel
Maurizio Benaglia
@ast
Maurizio Benaglia
@de
Maurizio Benaglia
@en
Maurizio Benaglia
@eo
Maurizio Benaglia
@es
Maurizio Benaglia
@fr
Maurizio Benaglia
@it
Maurizio Benaglia
@la
Maurizio Benaglia
@nl
Maurizio Benaglia
@pt
P1053
O-7692-2015
P106
P1153
7005112567
P21
P31
P3829
P496
0000-0002-9568-9642