Pierre Laszlo

ORCID: 0000-0003-4334-771X
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About
Contact & Profiles
Research Areas
  • Chemical Synthesis and Reactions
  • History and advancements in chemistry
  • Inorganic and Organometallic Chemistry
  • Various Chemistry Research Topics
  • Advanced NMR Techniques and Applications
  • NMR spectroscopy and applications
  • Molecular spectroscopy and chirality
  • Asymmetric Synthesis and Catalysis
  • Analytical Chemistry and Chromatography
  • Oxidative Organic Chemistry Reactions
  • Molecular Sensors and Ion Detection
  • Spectroscopy and Quantum Chemical Studies
  • Synthetic Organic Chemistry Methods
  • Mesoporous Materials and Catalysis
  • Chemical Synthesis and Analysis
  • Electrostatics and Colloid Interactions
  • Organic Chemistry Cycloaddition Reactions
  • Zeolite Catalysis and Synthesis
  • Catalysis and Oxidation Reactions
  • Molecular Junctions and Nanostructures
  • Sulfur-Based Synthesis Techniques
  • Historical and Scientific Studies
  • Polyoxometalates: Synthesis and Applications
  • Chemical Synthesis and Characterization
  • Asymmetric Hydrogenation and Catalysis

University of Liège
2001-2023

Bouygues (France)
2003-2021

École Polytechnique
1998-2020

Bibliothèque et Archives nationales du Québec
2017-2019

Laboratoire d'Informatique de l'École Polytechnique
1987-2018

Laboratoire de Chimie
1988-2012

Fondation de France
2010

Cornell University
1991-2010

Juniper Networks (United States)
2007

FirstHealth of the Carolinas
2002-2005

Layer aluminosilicates catalyze reactions in numerous ways. They stabilize high-energy intermediates. can store energy their lattice structures and release it the form of chemical energy. redox serve as photocatalytic devices. often exhibit high surface acidity. Organic that are catalyzed by agency days reviewed. The role clays prebiotic chemistry is also examined.

10.1126/science.235.4795.1473 article EN Science 1987-03-20

ADVERTISEMENT RETURN TO ISSUEPREVArticleCatalysis of organic reactions by inorganic solidsPierre LaszloCite this: Acc. Chem. Res. 1986, 19, 4, 121–127Publication Date (Print):April 1, 1986Publication History Published online1 May 2002Published inissue 1 April 1986https://pubs.acs.org/doi/10.1021/ar00124a004https://doi.org/10.1021/ar00124a004research-articleACS PublicationsRequest reuse permissionsArticle Views1282Altmetric-Citations288LEARN ABOUT THESE METRICSArticle Views are the...

10.1021/ar00124a004 article EN Accounts of Chemical Research 1986-04-01

A new, efficient preparation has been devised for potassium ferrate(VI) (K(2)FeO(4)). The ability of this high-valent iron salt oxidizing organic substrates in nonaqueous media was studied. Using benzyl alcohol as a model, the catalytic activity wide range microporous adsorbents ascertained. Among numerous solid supports aluminosilicate type, K10 montmorillonite clay found to be best at achieving quantitative formation benzaldehyde, without any overoxidation benzoic acid. roles various...

10.1021/jo960633p article EN The Journal of Organic Chemistry 1996-01-01

Just like glass flasks, beakers, and distillation columns, chemical structures are an integral part of our profession. We easily identified as chemists by how we draw formulas. Nonetheless, the simplicity these formulas—whether mere sketches or glossies fit for publication—is misleading. They pose numerous questions on ways represent structures. The picture right shows one way portraying a camphor molecule.

10.1002/anie.199100013 article EN Angewandte Chemie International Edition 1991-01-01

Partial dehydration in acetone activates iron(III) or copper(II) nitrate. These activated nitrato complexes, with covalent metal-ligand bonds, are stabilized a convenient form by impregnation upon modified montmorillonite clay (K10). mild and inexpensive reagents offer versatile applications to organic synthesis. As sources of nitrosonium cations (NO+), they perform number useful functional group interconversions. They effect also the regioselective mononitration phenols. 1. Introduction 2....

10.1055/s-1985-31382 article EN Synthesis 1985-01-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTAnalysis of the Nuclear, Magnetic Resonance Spectra Norbornene DerivativesPierre. Laszlo and Paul von Rague. SchleyerCite this: J. Am. Chem. Soc. 1964, 86, 6, 1171–1179Publication Date (Print):March 1, 1964Publication History Published online1 May 2002Published inissue 1 March 1964https://pubs.acs.org/doi/10.1021/ja01060a044https://doi.org/10.1021/ja01060a044research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/ja01060a044 article EN Journal of the American Chemical Society 1964-03-01

Abstract Catalysts are obtained by exchange of the interstitial cations in K10 montmorillonite. They applied to Friedel‐Crafts alkylations with halides, alcohols, and olefins. quite effective even unactivated hydrocarbons. Isomer distribution depends little on catalyst used. Thermodynamic equilibration does not take place, reactions appear be kinetically controlled. Efficiency catalysts bears no apparent relation that corresponding Lewis acids under homogeneous conditions, it nature...

10.1002/hlca.19870700310 article EN Helvetica Chimica Acta 1987-05-06

10.1016/0079-6565(67)80016-5 article EN Progress in Nuclear Magnetic Resonance Spectroscopy 1967-01-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTNew description of nuclear magnetic resonance solvent shifts for polar solutes in weakly associating aromatic solventsPierre Laszlo and Edward M. EnglerCite this: J. Am. Chem. Soc. 1971, 93, 6, 1317–1327Publication Date (Print):March 1, 1971Publication History Published online1 May 2002Published inissue 1 March 1971https://pubs.acs.org/doi/10.1021/ja00735a001https://doi.org/10.1021/ja00735a001research-articleACS PublicationsRequest reuse...

10.1021/ja00735a001 article EN Journal of the American Chemical Society 1971-03-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTElectronegativity of Substituents and Nuclear Magnetic Resonance Spectra Norbornene DerivativesPierre. Laszlo Paul von Rague. SchleyerCite this: J. Am. Chem. Soc. 1963, 85, 18, 2709–2712Publication Date (Print):September 1, 1963Publication History Published online1 May 2002Published inissue 1 September 1963https://pubs.acs.org/doi/10.1021/ja00901a006https://doi.org/10.1021/ja00901a006research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/ja00901a006 article EN Journal of the American Chemical Society 1963-09-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTMild and Selective Nitration by ClaycopBarbara Gigante, Angela O. Prazeres, Maria J. Marcelo-Curto, Andre Cornelis, Pierre LaszloCite this: Org. Chem. 1995, 60, 11, 3445–3447Publication Date (Print):June 1, 1995Publication History Published online1 May 2002Published inissue 1 June 1995https://pubs.acs.org/doi/10.1021/jo00116a034https://doi.org/10.1021/jo00116a034research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/jo00116a034 article EN The Journal of Organic Chemistry 1995-06-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTHeightened selectivity in aromatic nitrations and chlorinations by the use of solid supports catalystsLionel Delaude, Pierre Laszlo, Keith SmithCite this: Acc. Chem. Res. 1993, 26, 12, 607–613Publication Date (Print):December 1, 1993Publication History Published online1 May 2002Published inissue 1 December 1993https://doi.org/10.1021/ar00036a001Request reuse permissionsArticle Views556Altmetric-Citations104LEARN ABOUT THESE METRICSArticle Views are...

10.1021/ar00036a001 article EN Accounts of Chemical Research 1993-12-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTStereospecific cyclic ketone formation with iron(0): anatomy of an interligand reactionsEdward Weissberger and Pierre LaszloCite this: Acc. Chem. Res. 1976, 9, 6, 209–217Publication Date (Print):June 1, 1976Publication History Published online1 May 2002Published inissue 1 June 1976https://pubs.acs.org/doi/10.1021/ar50102a002https://doi.org/10.1021/ar50102a002research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/ar50102a002 article EN Accounts of Chemical Research 1976-06-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTDetermination of the acidity Lewis acidsPierre Laszlo and Michelle TestonCite this: J. Am. Chem. Soc. 1990, 112, 24, 8750–8754Publication Date (Print):November 1, 1990Publication History Published online1 May 2002Published inissue 1 November 1990https://pubs.acs.org/doi/10.1021/ja00180a017https://doi.org/10.1021/ja00180a017research-articleACS PublicationsRequest reuse permissionsArticle Views2657Altmetric-Citations107LEARN ABOUT THESE...

10.1021/ja00180a017 article EN Journal of the American Chemical Society 1990-11-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRole of alkali metal and ammonium cations in the self-assembly 5'-guanosine monophosphate dianionChristian Detellier Pierre LaszloCite this: J. Am. Chem. Soc. 1980, 102, 3, 1135–1141Publication Date (Print):January 1, 1980Publication History Published online1 May 2002Published inissue 1 January 1980https://pubs.acs.org/doi/10.1021/ja00523a033https://doi.org/10.1021/ja00523a033research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/ja00523a033 article EN Journal of the American Chemical Society 1980-01-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTProton, sodium-23, and phosphorus-31 NMR studies of the self-assembly 5'-guanosine monophosphate dianion in neutral aqueous solution presence sodium cationsMarie Borzo, Christian Detellier, Pierre Laszlo, Agnes ParisCite this: J. Am. Chem. Soc. 1980, 102, 3, 1124–1134Publication Date (Print):January 1, 1980Publication History Published online1 May 2002Published inissue 1 January...

10.1021/ja00523a032 article EN Journal of the American Chemical Society 1980-01-01

Natural clays can be modified into efficient and versatile catalysts for organic reactions. Among the assets of these heterogeneous are their lamellar swelling structure, large specific surfaces, availability both Brønsted- Lewis-acidic catalytic sites, low cost. 1. Introduction 2. Anionic Reactions 3. Diets-Alder 4. Acid-Catalyzed 5. Aromatic Chlorination 6. Using Metallic Nitrates 7. Conclusions

10.1055/s-1994-22775 article EN Synlett 1994-01-01

Abstract With the availability of Fourier transform spectrometers, 23 Na‐NMR spectroscopy has become an important tool. It affords direct insight into solvation and ion pairing phenomena, both in organic bio‐inorganic systems. Monitoring chemical shifts linewidths Na signals gives access to binding constants, reorientational correlation times microdynamics sodium coordination shell. The other cations can also be studied by spectroscopy, competition experiments.

10.1002/anie.197802541 article EN Angewandte Chemie International Edition 1978-04-01

Abstract 1,4‐Dihydropyridines can be aromatized under very mild conditions by K 10 Claysupported ferric and cupric nitrates.

10.1002/hlca.19840670834 article EN Helvetica Chimica Acta 1984-12-19
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