Year |
Citation |
Score |
2021 |
Hu L, Mahaut D, Tumanov N, Wouters J, Collard L, Robiette R, Berionni G. Sterically hindered -substituted phosphatriptycenes as configurationally stable -chirogenic triarylphosphines. Dalton Transactions (Cambridge, England : 2003). PMID 33729265 DOI: 10.1039/d1dt00816a |
0.685 |
|
2020 |
Doan TH, Chardon A, Osi A, Mahaut D, Tumanov N, Wouters J, Champagne B, Berionni G. Methylene Bridging Effect on the Structures, Lewis Acidities and Optical Properties of Semi-Planar Triarylboranes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32852852 DOI: 10.1002/Chem.202003319 |
0.421 |
|
2020 |
Chardon A, Osi A, Mahaut D, Doan TH, Tumanov N, Wouters J, Fusaro L, Champagne B, Berionni G. Controlled Generation of 9-Boratriptycene by Lewis Adduct Dissociation: Accessing a Unique Non-Planar Triarylborane. Angewandte Chemie (International Ed. in English). PMID 32324961 DOI: 10.1002/Anie.202003119 |
0.388 |
|
2020 |
Chardon A, Osi A, Mahaut D, Saida AB, Berionni G. Non-planar Boron Lewis Acids Taking the Next Step: Development of Tunable Lewis Acids, Lewis Superacids and Bifunctional Catalysts Synlett. DOI: 10.1055/S-0040-1707078 |
0.351 |
|
2019 |
Ben Saida A, Chardon A, Osi A, Tumanov N, Wouters J, Adjieufack AI, Champagne B, Berionni G. Pushing the Lewis Acidity Boundaries of Boron Compounds With Non-Planar Triarylboranes Derived from Triptycenes. Angewandte Chemie (International Ed. in English). PMID 31475396 DOI: 10.1002/Anie.201910908 |
0.411 |
|
2019 |
Hu L, Mahaut D, Tumanov N, Wouters J, Robiette R, Berionni G. Complementary Synthetic Approaches Toward 9-Phosphatriptycene and Structure-Reactivity Investigations of its Association with Sterically Hindered Lewis Acids. The Journal of Organic Chemistry. PMID 31385508 DOI: 10.1021/Acs.Joc.9B01570 |
0.695 |
|
2019 |
Anthore-Dalion L, Benischke AD, Wei B, Berionni G, Knochel P. The Halogen-Samarium Exchange Reaction. Synthetic Applications and Kinetics. Angewandte Chemie (International Ed. in English). PMID 30664831 DOI: 10.1002/Anie.201814373 |
0.759 |
|
2019 |
Anthore‐Dalion L, Benischke AD, Wei B, Berionni G, Knochel P. Die Halogen‐Samarium‐Austauschreaktion: Synthetische Anwendungen und Kinetik Angewandte Chemie. 131: 4086-4090. DOI: 10.1002/Ange.201814373 |
0.33 |
|
2017 |
Benischke AD, Anthore-Dalion L, Berionni G, Knochel P. Preparation of Functionalized Diaryl- and Diheteroaryl- Lanthanum Reagents via a Fast Halogen-Lanthanum Exchange. Angewandte Chemie (International Ed. in English). PMID 29052932 DOI: 10.1002/Anie.201709553 |
0.757 |
|
2017 |
García-Ruiz C, Chen JL, Sandford C, Feeney K, Lorenzo P, Berionni G, Mayr H, Aggarwal VK. Stereospecific Allylic Functionalization: The Reactivity of Allylboronate Complexes with Electrophiles. Journal of the American Chemical Society. PMID 29028321 DOI: 10.1021/Jacs.7B10240 |
0.559 |
|
2017 |
Issaian A, Faizi DJ, Bailey JO, Mayer P, Berionni G, Singleton DA, Blum SA. Mechanistic Studies of Formal Thioboration Reactions of Alkynes. The Journal of Organic Chemistry. PMID 28671461 DOI: 10.1021/Acs.Joc.7B01500 |
0.437 |
|
2017 |
Ganiek MA, Becker MR, Berionni G, Zipse H, Knochel P. Barbier Continuous Flow Preparation and Reactions of Carbamoyllithiums for Nucleophilic Amidation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28590518 DOI: 10.1002/Chem.201702593 |
0.499 |
|
2017 |
Follet E, Mayer P, Stephenson DS, Ofial AR, Berionni G. Reactivity-Tuning in Frustrated Lewis Pairs: Nucleophilicity and Lewis Basicity of Sterically Hindered Phosphines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28370848 DOI: 10.1002/Chem.201701080 |
0.69 |
|
2017 |
Lakhdar S, Berionni G, Terrier F. Superelectrophilicity in Michael-Type Reactions: Water Addition to 4-Nitrobenzodifuroxan Synthesis. 49: 3453-3459. DOI: 10.1055/S-0036-1590839 |
0.657 |
|
2017 |
Follet E, Zipse H, Lakhdar S, Ofial A, Berionni G. Nucleophilicities and Lewis Basicities of Sterically Hindered Pyridines Synthesis. 49: 3495-3504. DOI: 10.1055/S-0036-1590504 |
0.706 |
|
2017 |
Benischke AD, Anthore‐Dalion L, Berionni G, Knochel P. Herstellung von funktionalisierten Diaryl‐ und Diheteroaryl‐Lanthanreagenzien mittels eines schnellen Halogen‐Lanthan‐Austausches Angewandte Chemie. 129: 16608-16612. DOI: 10.1002/Ange.201709553 |
0.332 |
|
2016 |
Follet E, Mayer P, Berionni G. Structures, Lewis Acidities, Electrophilicities, and Protecting Group Abilities of Phenyl-Fluorenylium and Tritylium Ions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27723164 DOI: 10.1002/Chem.201603963 |
0.404 |
|
2016 |
Berionni G, Kurouchi H, Eisenburger L, Mayr H. Nucleophilicity of Alkyl Zirconocene and Titanocene Precatalysts and Kinetics of Activation by Carbenium Ions and by B(C₆F₅)₃. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27245119 DOI: 10.1002/Chem.201602452 |
0.577 |
|
2015 |
Morozova V, Mayer P, Berionni G. Scope and Mechanisms of Frustrated Lewis Pair Catalyzed Hydrogenation Reactions of Electron-Deficient C=C Double Bonds. Angewandte Chemie (International Ed. in English). 54: 14508-12. PMID 26493512 DOI: 10.1002/Anie.201507298 |
0.444 |
|
2015 |
Follet E, Berionni G, Mayer P, Mayr H. Structure and Reactivity of Indolylmethylium Ions: Scope and Limitations in Synthetic Applications. The Journal of Organic Chemistry. 80: 8643-56. PMID 26218059 DOI: 10.1021/Acs.Joc.5B01298 |
0.592 |
|
2015 |
Feeney K, Berionni G, Mayr H, Aggarwal VK. Structure and reactivity of boron-ate complexes derived from primary and secondary boronic esters. Organic Letters. 17: 2614-7. PMID 25973673 DOI: 10.1021/Acs.Orglett.5B00918 |
0.572 |
|
2015 |
Moriya K, Didier D, Simon M, Hammann JM, Berionni G, Karaghiosoff K, Zipse H, Mayr H, Knochel P. Stereoselective synthesis and reactions of secondary alkyllithium reagents functionalized at the 3-position. Angewandte Chemie (International Ed. in English). 54: 2754-7. PMID 25640227 DOI: 10.1002/Anie.201409165 |
0.754 |
|
2015 |
Berionni G, Leonov AI, Mayer P, Ofial AR, Mayr H. Fine-tuning the nucleophilic reactivities of boron ate complexes derived from aryl and heteroaryl boronic esters. Angewandte Chemie (International Ed. in English). 54: 2780-3. PMID 25604646 DOI: 10.1002/Anie.201410562 |
0.749 |
|
2015 |
Berionni G, Leonov AI, Mayer P, Ofial AR, Mayr H. Feineinstellung der nucleophilen Reaktivität von Bor-at-Komplexen aus Aryl- und Heteroarylboronsäureestern Angewandte Chemie. 127: 2820-2824. DOI: 10.1002/Ange.201410562 |
0.5 |
|
2015 |
Moriya K, Didier D, Simon M, Hammann JM, Berionni G, Karaghiosoff K, Zipse H, Mayr H, Knochel P. Stereoselektive Synthese und Reaktionen von in Position 3 funktionalisierten sekundären Alkyllithiumverbindungen Angewandte Chemie. 127: 2793-2796. DOI: 10.1002/Ange.201409165 |
0.696 |
|
2014 |
Chen X, Tan Y, Berionni G, Ofial AR, Mayr H. Di- and triarylmethylium ions as probes for the ambident reactivities of carbanions derived from 5-benzylated Meldrum's acid. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 11069-77. PMID 25099696 DOI: 10.1002/Chem.201403161 |
0.735 |
|
2014 |
Frischmuth A, Fernández M, Barl NM, Achrainer F, Zipse H, Berionni G, Mayr H, Karaghiosoff K, Knochel P. New in situ trapping metalations of functionalized arenes and heteroarenes with TMPLi in the presence of ZnCl2 and other metal salts. Angewandte Chemie (International Ed. in English). 53: 7928-32. PMID 24923789 DOI: 10.1002/Anie.201403688 |
0.555 |
|
2014 |
Dagousset G, Moriya K, Mose R, Berionni G, Karaghiosoff K, Knochel P. Diastereoselective synthesis of open-chain secondary alkyllithium compounds and trapping reactions with electrophiles. Angewandte Chemie (International Ed. in English). 53: 1425-9. PMID 24459059 DOI: 10.1002/Anie.201308679 |
0.531 |
|
2014 |
ElGuesmi N, Berionni G, Asghar BH. Mechanistic studies and quantification of the electrophilicity of aromatic triflones in σ-complexation and SNAr reactions Journal of Fluorine Chemistry. 160: 41-47. DOI: 10.1016/J.Jfluchem.2014.01.003 |
0.489 |
|
2014 |
Frischmuth A, Fernández M, Barl NM, Achrainer F, Zipse H, Berionni G, Mayr H, Karaghiosoff K, Knochel P. In-situ-Abfangmethode zur Metallierung funktionalisierter Arene und Heteroarene mit TMPLi in Gegenwart von ZnCl2und anderen Metallsalzen Angewandte Chemie. 126: 8062-8066. DOI: 10.1002/Ange.201403688 |
0.509 |
|
2013 |
El Guesmi N, Berionni G, Asghar BH. Electronic and solvent effects on kinetics of SAr substitution reactions of substituted anilines with 2,6-bis(trifluoromethanesulfonyl)-4-nitroanisole in MeOH-MeSO mixtures of varying composition: one reaction with two mechanistic pathways. Monatshefte Fur Chemie. 144: 1537-1545. PMID 26166874 DOI: 10.1007/S00706-013-1030-7 |
0.446 |
|
2013 |
Berionni G, Morozova V, Heininger M, Mayer P, Knochel P, Mayr H. Electrophilic aromatic substitutions of aryltrifluoroborates with retention of the BF3- group: quantification of the activating and directing effects of the trifluoroborate group. Journal of the American Chemical Society. 135: 6317-24. PMID 23534556 DOI: 10.1021/Ja4017655 |
0.59 |
|
2013 |
Dagousset G, Moriya K, Mose R, Berionni G, Karaghiosoff K, Knochel P. Diastereoselektive Synthese von offenkettigen sekundären Alkyllithiumverbindungen und Abfangreaktionen mit Elektrophilen Angewandte Chemie. 126: 1449-1453. DOI: 10.1002/Ange.201308679 |
0.427 |
|
2012 |
Maji B, Berionni G, Mayr H, Mayer P. 5-[(E)-Meth-oxy(phen-yl)methyl-idene]-1,3,4-triphenyl-4,5-dihydro-1H-1,2,4-triazole. Acta Crystallographica. Section E, Structure Reports Online. 68: o3307. PMID 23468812 DOI: 10.1107/S1600536812045692 |
0.625 |
|
2012 |
Berionni G, Mayer P, Mayr H. Potassium [1-(tert-but-oxy-carbon-yl)-1H-indol-3-yl]trifluoro-borate hemihydrate. Acta Crystallographica. Section E, Structure Reports Online. 68: m551-2. PMID 22590073 DOI: 10.1107/S1600536812014225 |
0.482 |
|
2012 |
Berionni G, Maji B, Knochel P, Mayr H. Nucleophilicity parameters for designing transition metal-free C-C bond forming reactions of organoboron compounds Chemical Science. 3: 878-882. DOI: 10.1039/C2Sc00883A |
0.714 |
|
2011 |
De Rycke N, Berionni G, Couty F, Mayr H, Goumont R, David OR. Synthesis and reactivity of highly nucleophilic pyridines. Organic Letters. 13: 530-3. PMID 21186828 DOI: 10.1021/Ol1029589 |
0.555 |
|
2011 |
Berionni G, Gonçalves AM, Mathieu C, Devic T, Etchéberry A, Goumont R. Electrochemical and spectrophotometrical investigation of the electron-accepting strength of organic superelectrophiles: X-ray structure of their charge transfer complexes with tetrathiafulvalene. Physical Chemistry Chemical Physics : Pccp. 13: 2857-69. PMID 21165467 DOI: 10.1039/C0Cp01282C |
0.322 |
|
2011 |
Lakhdar S, Berionni G, Goumont R, Terrier F. Understanding the diels-alder reactivity of superelectrophilic nitrobenzofuroxans and related 10π-heteroaromatics through DFT-based electrophilicity Letters in Organic Chemistry. 8: 108-118. DOI: 10.2174/157017811794697412 |
0.644 |
|
2011 |
Berionni G, Branca M, Pégot B, Marrot J, Kizilian E, Goumont R. The N‐Alkylation of Substituted 4‐Tetrazolo[1,5‐a]pyridines: Easy Access to a New Series of Electrophiles European Journal of Organic Chemistry. 2011: 5104-5113. DOI: 10.1002/Ejoc.201100595 |
0.427 |
|
2010 |
Lakhdar S, Terrier F, Vichard D, Berionni G, El Guesmi N, Goumont R, Boubaker T. The Diels-Alder reaction of 4,6-dinitrobenzofuroxan with 1-trimethylsilyloxybuta-1,3-diene: a case example of a stepwise cycloaddition. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 5681-90. PMID 20376824 DOI: 10.1002/Chem.200903008 |
0.688 |
|
2010 |
Berionni G, Pégot B, Goumont R. Theoretical and experimental 1H, 13C and 15N NMR studies of N-alkylation of substituted tetrazolo[1,5-a]pyridines. Magnetic Resonance in Chemistry : Mrc. 48: 101-10. PMID 19937909 DOI: 10.1002/Mrc.2544 |
0.36 |
|
2009 |
Berionni G, Pégot B, Marrot J, Goumont R. Supramolecular association of 1,2,5-chalcogenadiazoles: an unexpected self-assembled dissymetric [Se⋯N]2 four-membered ring Crystengcomm. 11: 986-988. DOI: 10.1039/B820258C |
0.305 |
|
2007 |
Lakhdar S, Goumont R, Berionni G, Boubaker T, Kurbatov S, Terrier F. Superelectrophilicity of the nitroolefinic fragment of 4-nitrobenzodifuroxan in Michael-type reactions with indoles: a kinetic study in acetonitrile. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 8317-24. PMID 17642071 DOI: 10.1002/Chem.200700676 |
0.677 |
|
2007 |
Micheletti G, Pollicino S, Ricci A, Berionni G, Cahiez G. Michael addition of manganese enolates to nitroolefins Synlett. 2829-2832. DOI: 10.1055/S-2007-991096 |
0.419 |
|
Low-probability matches (unlikely to be authored by this person) |
2014 |
Berionni G, Wu JI, Schleyer PV. Aromaticity evaluations of planar [6]radialenes. Organic Letters. 16: 6116-9. PMID 25409485 DOI: 10.1021/Ol5029699 |
0.294 |
|
2023 |
Osi A, Tumanov N, Fusaro L, Wouters J, Berionni G, Chardon A. From Proton to Boron: The Lewis Analogs of Protonated Brønsted Super Acids. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301146. PMID 37078439 DOI: 10.1002/chem.202301146 |
0.285 |
|
2009 |
Berionni G, Bertelle PA, Marrot J, Goumont R. X-ray structure of a CT complex relevant to Diels-Alder reactivity of anthracenes. Journal of the American Chemical Society. 131: 18224-5. PMID 19968279 DOI: 10.1021/Ja908747J |
0.275 |
|
2021 |
Gama M, Antognini Silva X, Doan T, Osi A, Chardon A, Tumanov N, Wouters J, Berionni G. Triptycene Boronates, Boranes, and Boron Ate‐Complexes: Toward Sterically Hindered Triarylboranes and Trifluoroborates European Journal of Organic Chemistry. 2021: 1440-1445. DOI: 10.1002/EJOC.202001672 |
0.273 |
|
2020 |
Chardon A, Osi A, Mahaut D, Doan TH, Tumanov N, Wouters J, Fusaro L, Champagne B, Berionni G. Innentitelbild: Controlled Generation of 9-Boratriptycene by Lewis Adduct Dissociation: Accessing a Non-Planar Triarylborane (Angew. Chem. 30/2020) Angewandte Chemie. 132: 12322-12322. DOI: 10.1002/Ange.202007536 |
0.267 |
|
2020 |
Chardon A, Osi A, Mahaut D, Doan T, Tumanov N, Wouters J, Fusaro L, Champagne B, Berionni G. Inside Cover: Controlled Generation of 9‐Boratriptycene by Lewis Adduct Dissociation: Accessing a Non‐Planar Triarylborane (Angew. Chem. Int. Ed. 30/2020) Angewandte Chemie. 59: 12226-12226. DOI: 10.1002/Anie.202007536 |
0.251 |
|
2021 |
Mahaut D, Chardon A, Mineur L, Berionni G, Champagne B. Rational Development of a Metal-Free Bifunctional System for the C-H Activation of Methane: A Density Functional Theory Investigation. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. PMID 34309144 DOI: 10.1002/cphc.202100527 |
0.239 |
|
2008 |
Micheletti G, Pollicino S, Ricci A, Berionni G, Cahiez G. ChemInform Abstract: Michael Addition of Manganese Enolates to Nitroolefins. Cheminform. 39. DOI: 10.1002/chin.200811067 |
0.234 |
|
2021 |
Osi A, Mahaut D, Tumanov N, Fusaro L, Wouters J, Champagne B, Chardon A, Berionni G. Taming the Lewis Superacidity of Non-Planar Boranes: C-H Bond Activation and Non-Classical Binding Modes at Boron. Angewandte Chemie (International Ed. in English). PMID 34623002 DOI: 10.1002/anie.202112342 |
0.224 |
|
2022 |
Berionni G. Regioselective Transition-Metal-Free Arene C-H Borylations: From Directing Groups to Borylation Template Reagents. Angewandte Chemie (International Ed. in English). 61: e202210284. PMID 36026558 DOI: 10.1002/anie.202210284 |
0.198 |
|
2022 |
Mahaut D, Berionni G, Champagne B. 9-Phosphatriptycene Derivatives: From Their Weak Basicity to Their Application in Frustrated Lewis Pair Chemistry. The Journal of Physical Chemistry. A. PMID 35507420 DOI: 10.1021/acs.jpca.2c01339 |
0.194 |
|
2023 |
Berionni G. A focus on anionic boron anthracenes and triptycenes as entry point toward B-doped polyaromatic materials and Lewis acids. Chemical Science. 14: 5241-5242. PMID 37234905 DOI: 10.1039/d3sc90074f |
0.184 |
|
2023 |
Berionni G. Controlling precision on the ring. Science (New York, N.Y.). 382: 1122-1123. PMID 38060642 DOI: 10.1126/science.adl4860 |
0.159 |
|
2020 |
Chardon A, Osi A, Mahaut D, Doan T, Tumanov N, Wouters J, Fusaro L, Champagne B, Berionni G. Controlled Generation of 9‐Boratriptycene by Lewis Adduct Dissociation: Accessing a Non‐Planar Triarylborane Angewandte Chemie. 132: 12502-12506. DOI: 10.1002/ange.202003119 |
0.115 |
|
2021 |
Ngo Nyobe JC, Tekapi Tsopgni WD, Longue Ekon JP, Ben Saida A, Djuidje AG, Bengondo AB, Etame Loe G, Berionni G, Mama DB, Ndom JC, Mpondo EM. Chemical constituents from Psychotria arborea Hiern (Rubiaceae) Biochemical Systematics and Ecology. 94: 104212. DOI: 10.1016/j.bse.2020.104212 |
0.069 |
|
Hide low-probability matches. |