Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Olivier Perraud"'
Autor:
Augustin Long, Olivier Perraud, Erwann Jeanneau, Christophe Aronica, Jean-Pierre Dutasta, Alexandre Martinez
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1885-1889 (2018)
A hemicryptophane cage bearing amine and amide functions in its three linkers was synthesized in five steps. The X-ray molecular structure of the cage shows a triple-stranded helical arrangement of the linkers stabilized by intramolecular hydrogen bo
Externí odkaz:
https://doaj.org/article/9229e014552d4472b18a0c92778f54a8
Autor:
Marianna Rondon, Yoldes Khabzina, Alejandro Orsikowsky, Jean-Benoit Laudet, He Zhao, Olivier Perraud, Emil Gyllenhammar, Jostein Kolbu
Publikováno v:
Day 1 Mon, May 02, 2022.
In the current energy transition scenario, gas represents one of the main pillars for a greener energy mix. In 2015, we presented two promising schemes to produce a challenging notional gas field located 2500 meters water depth and 300 km from shore
Autor:
Jean-Pierre Dutasta, Alexandre Martinez, Olivier Perraud, Vincent Robert, Augustin Long, Muriel Albalat
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2018, 83 (12), pp.6301-6306. ⟨10.1021/acs.joc.8b00276⟩
Journal of Organic Chemistry, 2018, 83 (12), pp.6301-6306. ⟨10.1021/acs.joc.8b00276⟩
Journal of Organic Chemistry, American Chemical Society, 2018, 83 (12), pp.6301-6306. ⟨10.1021/acs.joc.8b00276⟩
Journal of Organic Chemistry, 2018, 83 (12), pp.6301-6306. ⟨10.1021/acs.joc.8b00276⟩
International audience; A new chiral hemicryptophane cage combining an electron-rich cyclotriveratrylene (CTV) unit and polar amine functions has been synthesized. The resolution of the racemic mixture has been performed by chiral HPLC, and the assig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a0f13b5c20cf3812e6a8cc82273f283
https://hal.archives-ouvertes.fr/hal-01896109
https://hal.archives-ouvertes.fr/hal-01896109
Autor:
Dawei Zhang, Vincent Robert, Jean-Pierre Dutasta, Eloisa Serrano, Bastien Chatelet, Olivier Perraud, Alexandre Martinez
Publikováno v:
ChemPhysChem
ChemPhysChem, 2015, 16 (14), pp.2931-2935. ⟨10.1002/cphc.201500610⟩
ChemPhysChem, Wiley-VCH Verlag, 2015, 16 (14), pp.2931-2935. ⟨10.1002/cphc.201500610⟩
ChemPhysChem, 2015, 16 (14), pp.2931-2935. ⟨10.1002/cphc.201500610⟩
ChemPhysChem, Wiley-VCH Verlag, 2015, 16 (14), pp.2931-2935. ⟨10.1002/cphc.201500610⟩
International audience; The recognition properties of heteroditopic hemicryptophane hosts towards anions, cations, and neutral pairs, combining both cation-pi and anion-pi interaction sites, were investigated to probe the complexity of interfering we
Autor:
Lhoussain Khrouz, Jean-Pierre Dutasta, Laurent Bonneviot, Belén Albela, Vincent Robert, Alexandre Martinez, Olivier Perraud, Jean-Bernard Tommasino
Publikováno v:
Dalton Transactions
Dalton Transactions, Royal Society of Chemistry, 2013, 42 (5), pp.1530-1535. ⟨10.1039/c2dt31530k⟩
Dalton Transactions, 2013, 42 (5), pp.1530-1535. ⟨10.1039/c2dt31530k⟩
Dalton Transactions, Royal Society of Chemistry, 2013, 42 (5), pp.1530-1535. ⟨10.1039/c2dt31530k⟩
Dalton Transactions, 2013, 42 (5), pp.1530-1535. ⟨10.1039/c2dt31530k⟩
International audience; Three copper(II)@hemicryptophane complexes with various cavity sizes and shapes, Cu(II)@1, Cu(II)@2 and Cu(II)@3, were synthesized and characterized by near-IR/vis and EPR spectroscopies. The spectroscopic data are consistent
Autor:
Christophe Aronica, Olivier Perraud, Jean-Pierre Dutasta, Alexandre Martinez, Pascal Dimitrov Raytchev
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2010, 75 (6), pp.2099-2102. ⟨10.1021/jo100052r⟩
Journal of Organic Chemistry, 2010, 75 (6), pp.2099-2102. ⟨10.1021/jo100052r⟩
Journal of Organic Chemistry, American Chemical Society, 2010, 75 (6), pp.2099-2102. ⟨10.1021/jo100052r⟩
Journal of Organic Chemistry, 2010, 75 (6), pp.2099-2102. ⟨10.1021/jo100052r⟩
International audience; The first hemicryptophanes derived from tris(N-alkyl-carbamoylmethyl)amine and tris(2-aminoethyl)amine (tren) have been synthesized following a single synthetic pathway that allows the subsequent formation of the two heterodit
Autor:
Benjamin Bousquet, Aline Schmitt, Marion Valls, Elina Payet, Daniele Padula, Bastien Chatelet, Jean-Pierre Dutasta, Lorenzo Di Bari, Olivier Perraud, Alexandre Martinez
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2014, 12 (24), pp.4211-4217. ⟨10.1039/c4ob00156g⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2014, 12 (24), pp.4211-4217. ⟨10.1039/c4ob00156g⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2014, 12 (24), pp.4211-4217. ⟨10.1039/c4ob00156g⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2014, 12 (24), pp.4211-4217. ⟨10.1039/c4ob00156g⟩
International audience; Four new enantiomerically and diastereomerically pure hemicryptophane hosts (M-SSS-2/P-SSS-2 and M-RRR-2/P-RRR-2 pairs) were designed for the recognition of sugar derivatives. Their absolute configuration was determined from t
Publikováno v:
Organic letters, 14(21), 5404-5407. AMER CHEMICAL SOC INC
Designing synthetic receptors that bind biologically relevant guests in an aqueous solution remains a considerable challenge. We now report a new synthetic receptor for nicotine, selected from a dynamic combinatorial library, that binds this guest in
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2012, 10 (5), pp.1056-1059. ⟨10.1039/c1ob06657a⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2012, 10 (5), pp.1056-1059. ⟨10.1039/c1ob06657a⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2012, 10 (5), pp.1056-1059. ⟨10.1039/c1ob06657a⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2012, 10 (5), pp.1056-1059. ⟨10.1039/c1ob06657a⟩
International audience; Hemicryptophane 3 was found to be an efficient and selective primary alkylammonium receptor. Binding constants are 1000-fold higher than those previously reported for hemicryptophane hosts. Efficient complexation of dopamine e
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, 2011, 17 (48), pp.13405-13408. ⟨10.1002/chem.201101522⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2011, 17 (48), pp.13405-13408. ⟨10.1002/chem.201101522⟩
Chemistry-A European Journal, 2011, 17 (48), pp.13405-13408. ⟨10.1002/chem.201101522⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2011, 17 (48), pp.13405-13408. ⟨10.1002/chem.201101522⟩
International audience; The perfect host: Hemicryptophane 1 selectively binds taurine neurotransmitters in CD3CN/D2O. Association constants determined by DOSY NMR spectroscopy demonstrate that this recognition is highly selective over other related s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb84abc4466490f1a61bd5520715da60
https://hal.science/hal-01116909
https://hal.science/hal-01116909