Search Results - "Lapis, Alexandre A.M."
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Supported Ionic Liquid Enzymatic Catalysis for the Production of Biodiesel
Published in Advanced synthesis & catalysis (04-01-2008)“…Pseudomonas cepacia lipase supported in the 1‐n‐butyl‐3‐methylimidazolium bis(trifluoromethylsulfonyl)imide ionic liquid is an alternative “green” method for…”
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1- n-Butyl-3-methylimidazolium tetrachloro-indate ( BMI ⋅ InCl 4 ) as a media for the synthesis of biodiesel from vegetable oils
Published in Journal of catalysis (25-07-2007)“…The complex [Sn(3-hydroxy-2-methyl-4-pyrone) 2(H 2O) 2] immobilized in 1- n-butyl-3-methylimidazolium tetrachloro-indate ( BMI ⋅ InCl 4 ) ionic liquid forms an…”
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3
Studies on the Eschenmoser coupling reaction and insights on its mechanism. Application in the synthesis of Norallosedamine and other alkaloids
Published in Tetrahedron (21-03-2009)“…The conditions of the Eschenmoser coupling reaction were studied. The formation of the α-thioiminium ion was achieved faster in the presence of an additive…”
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4
Ionic Liquid Supported Acid/Base-Catalyzed Production of Biodiesel
Published in ChemSusChem (01-09-2008)“…The transesterification (alcoholysis) reaction was successfully applied to synthesize biodiesel from vegetable oils using imidazolium‐based ionic liquids under…”
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5
On the use of 2,1,3-benzothiadiazole derivatives as selective live cell fluorescence imaging probes
Published in Bioorganic & medicinal chemistry letters (15-10-2010)“…Newly designed 2,1,3-benzothiadiazole-containing fluorescent probes with four excited state intramolecular proton transfer (ESIPT) sites were successfully…”
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Asymmetric reduction of prochiral ketones using in situ generated oxazaborolidine derived from (1 S,2 S,3 R,4 R)-3-amino-7,7-dimethoxynorbornan-2-ol. An efficient synthesis of enantiopure ( R)-tomoxetine
Published in Tetrahedron letters (01-01-2005)“…In this work, we report our results on the asymmetric reduction of prochiral aromatic and aliphatic ketones 3 , 5– 8 catalyzed by the novel in situ generated…”
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2,1,3-Benzothiadiazole and Derivatives: Synthesis, Properties, Reactions, and Applications in Light Technology of Small Molecules
Published in European journal of organic chemistry (01-01-2013)“…2,1,3‐Benzothiadiazole (BTD) is one of the most important nuclei used in the chemistry of photoluminescent compounds and applicable for light technology. The…”
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Functional chromophores synthesized via multicomponent Reactions: A review on their use as cell-imaging probes
Published in Methods (San Diego, Calif.) (01-12-2023)“…This review aims to provide a comprehensive overview of recent advancements and applications of fluorescence imaging probes synthesized via MCRs…”
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What do we know about the ionic liquid effect in catalyzed multicomponent reactions?: A critical review
Published in Current opinion in green and sustainable chemistry (01-06-2022)“…Several multicomponent reactions (MCRs) have been conducted with improved yields and selectivities when ionic liquids (ILs) were applied as the catalysts or…”
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Recent developments in the chemistry of deoxyribonucleic acid (DNA) intercalators: principles, design, synthesis, applications and trends
Published in Molecules (07-05-2009)“…In the present overview, we describe the bases of intercalation of small molecules (cationic and polar neutral compounds) in DNA. We briefly describe the…”
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Charge-Tagged Acetate Ligands As Mass Spectrometry Probes for Metal Complexes Investigations: Applications in Suzuki and Heck Phosphine-Free Reactions
Published in Journal of organic chemistry (16-12-2011)“…An acetate anion bearing an imidazolium cation as its charge tag was reacted with M(OAc)2 complexes (where M = Ni, Cu, and Pd; in situ reaction) to form…”
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Intermolecular hydroamination and hydroarylation reactions of alkenes in ionic liquids
Published in Tetrahedron letters (18-09-2006)“…Intermolecular hydroamination or hydroarylation reactions of norbornene and cyclohexadiene performed with catalytic amounts of Brönsted or Lewis acid in ionic…”
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13
New Sensitive Fluorophores for Selective DNA Detection
Published in Organic letters (27-09-2007)“…4,7-Disubstituted benzothiadiazoles containing 1-arylethynyl and 4-methoxyphenyl groups are selective photoluminescent “light up” probes to duplex DNA with…”
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14
Designed non-symmetrical 4,7-pi-extended-2,1,3-benzothiadiazole derivatives: Synthesis guided by DFT predictions
Published in Journal of physical organic chemistry (01-04-2014)“…A series of rationally designed, non‐symmetrical, 4,7‐π‐extended‐2,1,3‐benzothidiazole derivatives had their electronic and geometrical properties evaluated by…”
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Steady-state kinetics of indole-3-glycerol phosphate synthase from Mycobacterium tuberculosis
Published in Archives of biochemistry and biophysics (01-06-2009)“…Indole-3-glycerol phosphate synthase (IGPS) catalyzes the irreversible ring closure of 1-( o-carboxyphenylamino)-1-deoxyribulose 5-phosphate (CdRP), through…”
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Nickel-containing di-charged imidazolium ligand with high crystalline organization. Interception and characterization of a transient carbene/cation species
Published in Inorganica Chimica Acta (15-05-2011)“…New nickel-containing di-charged imidazolium ligand was prepared by treatment of nickel chloride with bis-(2-(3-methylimidazolium-1-yl)ethyl)ether dichloride…”
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On the selective detection of duplex deoxyribonucleic acids by 2,1,3-benzothiadiazole fluorophores
Published in Molecular bioSystems (01-01-2010)“…A series of 4,7-pi-extended 2,1,3-benzothiadiazoles (BTDs) with different molecular architectures, in particular, the organic dyes based on the…”
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18
The catalytic mechanism of indole-3-glycerol phosphate synthase (IGPS) investigated by electrospray ionization (tandem) mass spectrometry
Published in Tetrahedron letters (06-10-2008)“…The catalytic mechanism indole ring closure promoted by IGPS enzyme was studied by ESI mass spectrometry. An enzymatic reaction has been monitored by on-line…”
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19
An efficient synthesis of enantiopure (+)- and (−)-3- exo-amino-7,7-dimethoxynorbornan-2- exo-ols
Published in Tetrahedron: asymmetry (19-03-2001)“…We describe the synthesis of new amino alcohols (+)- and (−)-3- exo-amino-7,7-dimethoxynorbonan-2- exo-ols. The (+)- or…”
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