Výsledky vyhledávání - "François Porzio"

A strategic approach to the synthesis of functionalized spirooxindole pyrrolidine derivatives: in vitro antibacterial, antifungal, antimalarial and antitubercular studies

Autor: Yoann Rousselin, François Porzio, Dhanji P. Rajani, M. M. Kubicki, Saoussen Haddad, Tarunkumar Nanjibhai Akhaja, Sarra Boudriga, Armand Soldera, Michael Knorr, Jignesh P. Raval, Moheddine Askri

Publikováno v: New Journal of Chemistry. 39:520-528

A series of spiro[pyrrolidin-2,3′-oxindoles] has been synthesized by exo-selective 1,3-dipolar cycloaddition reaction of a stabilized azomethine ylide, generated in situ by thermal [1,5]-prototropy, across various (E)-3-arylidene-1-phenyl-pyrrolidi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4e16fc0e070bcf32f2a5010e56bbb611
https://doi.org/10.1039/c4nj01008f

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Mechanical equilibrium, a prerequisite to unveil auxetic properties in molecular compounds

Autor: Armand Soldera, R. S. Underhill, Stéphane Tesson, François Porzio, Étienne Cuierrier, Clément Wespiser

Publikováno v: Molecular Simulation
Molecular Simulation, Taylor & Francis, 2017, 43 (3), pp.169--175. ⟨10.1080/08927022.2016.1241397⟩

International audience; The unique physical properties of auxetic compounds make them very attractive materials. Nevertheless, no synthesised materials known to exhibit negative Poisson’s ratio at the molecular level have been made. One way to expl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a7504a20a104fae70d27a25f4a2a730
https://hal.archives-ouvertes.fr/hal-01515650

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New Insights into the Thermal Stability of the Smectic C Phase

Autor: Armand Soldera, Etienne Levert, François Porzio, Richard Vadnais

Publikováno v: The Journal of Physical Chemistry B. 118:4037-4043

Subtle differences in the molecular structure of mesogens can lead to very different experimental polymorphisms. The smectic C (SmC) phase can actually be exhibited by one isomer and not the other, or the range of temperature can be completely differ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bce4e1c8604332678f0c0b72645ced5f
https://doi.org/10.1021/jp5011605

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Synthesis of novel dispiropyrrolothiazoles by three-component 1,3-dipolar cycloaddition and evaluation of their antimycobacterial activity

Autor: Perumal Yogeeswari, Yoann Rousselin, François Porzio, Marek M. Kubicki, Michael Knorr, Saoussen Haddad, Sarra Boudriga, Armand Soldera, Moheddine Askri, Dharmarajan Sriram

Publikováno v: RSC Advances
RSC Advances, Royal Society of Chemistry, 2014, 4, pp.59462-59471. ⟨10.1039/C4RA11940A⟩

In an on-going effort to develop novel anti-tubercular agents, a series of original dispiropyrrolothiazole derivatives have been synthesized by three-component 1,3-dipolar cycloaddition of (E)-3-arylidene-1-phenyl-pyrrolidine-2,5-diones, 1,3-thiazola

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9c7ed5dcf86807643ce1ee7100e3d4c
https://doi.org/10.1039/c4ra11940a

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Chapter 11. Molecular Simulation of Fluorinated Telomer and Polymers

Autor: Alexandre Fleury, Étienne Cuierrier, François Porzio, Bruno Ameduri, Armand Soldera

Despite the omnipresence in everyday life of fluoropolymers, mainly due to their numerous and attractive applications, further progress in their synthesis is needed. Experimentally, the study of telomers is of great interest, with the aim of better c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::31a176011a7e59325b9697f80641b33e
https://doi.org/10.1039/9781782626718-00359

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ChemInform Abstract: Regio- and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines Through Azomethine Ylide Cycloaddition Reaction

Autor: Sarra Boudriga, Moheddine Askri, François Porzio, Marek M. Kubicki, Saoussen Haddad, Carsten Strohmann, Michael Knorr, Armand Soldera, Christopher Golz, Yoann Rousselin

Publikováno v: ChemInform. 47

A series of original spiropyrrolizidine derivatives has been prepared by a one-pot three-component [3 + 2] cycloaddition reaction of (E)-3-arylidene-1-phenyl-pyrrolidine-2,5-diones, l-proline, and the cyclic ketones 1H-indole-2,3-dione (isatin), inde

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c94764ba0ff5ca6fc2f3bfab6bea7069
https://doi.org/10.1002/chin.201605117

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Molecular Dynamics Simulation of the SmC Phase

Autor: François Porzio, Etienne Levert, Armand Soldera

Publikováno v: Ferroelectrics. 431:121-128

The smectic C phase of a family of calamitic rod-like chiral mesogens was investigated using all-atom molecular dynamics simulation. The studied molecules differ from each other by the orientation of an ester moiety inside the rigid core, the nature

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f3868e93f6c0704a7d8085cf1078fe5d
https://doi.org/10.1080/00150193.2012.684972

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Regio- and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines through Azomethine Ylide Cycloaddition Reaction

Autor: Armand Soldera, Sarra Boudriga, Moheddine Askri, Christopher Golz, Marek M. Kubicki, Saoussen Haddad, Michael Knorr, Carsten Strohmann, François Porzio, Yoann Rousselin

Publikováno v: Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2015, 80, pp. 9064-9075. ⟨10.1021/acs.joc.5b01399⟩

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f8ca51073efa8f6bd547fa880a47339
https://pubmed.ncbi.nlm.nih.gov/26291879

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ChemInform Abstract: Synthesis of Novel Dispiropyrrolothiazoles by Three-Component 1,3-Dipolar Cycloaddition and Evaluation of Their Antimycobacterial Activity

Autor: Armand Soldera, François Porzio, Marek M. Kubicki, Yoann Rousselin, Moheddine Askri, Michael Knorr, Saoussen Haddad, Perumal Yogeeswari, Sarra Boudriga, Dharmarajan Sriram

Publikováno v: ChemInform. 46

Novel dispiropyrrolothiazole derivatives (IV) and (VI) are synthesized under mild reaction conditions in a complete regio- and stereoselective manner using three-component 1,3-dipolar cycloaddition reactions of cyclic diketones (I) or (V) with thiazo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::be80b130a695ca15f6cce2ca8fda3e74
https://doi.org/10.1002/chin.201518118

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