Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Virginie Héran"'
Autor:
Virginie Héran, Raphaël Rahmani, Béatrice Tuccio, Laurent Commeiras, Jean-Luc Parrain, Yannick Carissan, Romain Blanc, Jean Drujon
Publikováno v:
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2014, 16, pp.7513-7520. ⟨10.1039/c3cp55077j⟩
Physical Chemistry Chemical Physics, 2014, 16, pp.7513-7520. ⟨10.1039/c3cp55077j⟩
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2014, 16, pp.7513-7520. ⟨10.1039/c3cp55077j⟩
Physical Chemistry Chemical Physics, 2014, 16, pp.7513-7520. ⟨10.1039/c3cp55077j⟩
International audience; The auto-oxidation of trans-1,2-disiloxybenzocyclobutene was found to be very efficient, giving endoperoxide in quantitative yield. Each step of the mechanism of spin-forbidden addition of triplet oxygen O2 was studied by both
Autor:
Jean-Marc Pons, Cyril Bressy, Sabrina Parat, Mathieu Candy, Hugues Bienaymé, Loïc Tomas, Virginie Héran
Publikováno v:
Chemistry - A European Journal. 18:14267-14271
The key is symmetry! A convergent synthetic approach of the highly cytotoxic natural product (-)-callystatin A was developed assembling three fragments through Julia-Kocienski olefination and Stille cross-coupling. The new strategy relies on a pivota
Autor:
Mohamed Abarbri, Jean-Luc Parrain, Khalil Cherry, Jérôme Thibonnet, Virginie Héran, Alain Duchêne, Laurent Commeiras, Samuel Inack Ngi
Publikováno v:
ChemInform. 43
Autor:
Mohamed Abarbri, Jérôme Thibonnet, Jean-Luc Parrain, A. Duchene, Samuel Inack Ngi, Khalil Cherry, Laurent Commeiras, Virginie Héran
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2011, 17 (49), pp.13692-13696. ⟨10.1002/chem.201102570⟩
Chemistry-A European Journal, 2011, 17 (49), pp.13692-13696. ⟨10.1002/chem.201102570⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2011, 17 (49), pp.13692-13696. ⟨10.1002/chem.201102570⟩
Chemistry-A European Journal, 2011, 17 (49), pp.13692-13696. ⟨10.1002/chem.201102570⟩
International audience; An easy and mild copper(I)-catalysed lactonisation of readily available (E)-2,3-dihalopropenoic acid derivatives regio- and stereoselectively leads to rarely described (Z)-3-halo-5-ylidene-5H-furan-2-ones. These compounds are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae12b1462441108d15c2c4ab4fdc49ff
https://hal.archives-ouvertes.fr/hal-00738084
https://hal.archives-ouvertes.fr/hal-00738084
Publikováno v:
ChemInform. 42
An efficient synthesis of deoxy-lambertellols proceeds through a highly chemo- and diastereoselective Diels—Alder cycloaddition.
Autor:
Raphael Mathey, Frédéric Mallard, Mathieu Dupoy, Armelle Novelli-Rousseau, Jean-Pierre Moy, Florence Rivera, Sophie Morales, Pierre Marcoux, Virginie Héran, Pierre L. Joly
Publikováno v:
Colloids and Surfaces A: Physicochemical and Engineering Aspects
Colloids and Surfaces A: Physicochemical and Engineering Aspects, Elsevier, 2011, 377, pp.54-62. ⟨10.1016/j.colsurfa.2010.12.013⟩
Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2011, 377, pp.54-62. ⟨10.1016/j.colsurfa.2010.12.013⟩
Colloids and Surfaces A: Physicochemical and Engineering Aspects, Elsevier, 2011, 377, pp.54-62. ⟨10.1016/j.colsurfa.2010.12.013⟩
Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2011, 377, pp.54-62. ⟨10.1016/j.colsurfa.2010.12.013⟩
Today, rapid detection and identification of bacteria in microbiological diagnosis is a major issue. Reference methods usually rely on growth of microorganisms, with the drawback of lengthy time-to-result. The method provides global information on a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6520bc53c99adba79a23b3186eb9abd
https://hal-cea.archives-ouvertes.fr/cea-00822878/document
https://hal-cea.archives-ouvertes.fr/cea-00822878/document
Publikováno v:
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2010, 8, pp.5490-5494
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2010, 8, pp.5490-5494
Organic & Biomolecular Chemistry, 2010, 8, pp.5490-5494
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2010, 8, pp.5490-5494
International audience; An efficient synthesis of deoxy-lambertellols was reported through a highly chemo- and diastereoselective intermolecular Diels-Alder cycloaddition between trans-1,2-disiloxybenzocyclobutenes and 2-methylproto- anemonine. Such
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ced2fcbe9c04d2ef5d583c710847d8c
https://hal.science/hal-00682615/file/HAL22.pptx.pdf
https://hal.science/hal-00682615/file/HAL22.pptx.pdf
Autor:
Romain Blanc, Jérôme Thibonnet, Sébastien Dubois, Virginie Héran, Jean-Luc Parrain, Raphaël Rahmani, Fabien Rodier, Laurent Commeiras
Publikováno v:
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2012, 10, pp.4712-4719. ⟨10.1039/c2ob25299f⟩
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2012, 10, pp.4712-4719. ⟨10.1039/c2ob25299f⟩
Organic & Biomolecular Chemistry, 2012, 10, pp.4712-4719. ⟨10.1039/c2ob25299f⟩
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2012, 10, pp.4712-4719. ⟨10.1039/c2ob25299f⟩
International audience; An efficient and rapid synthesis of the CDEF ring system of lactonamycinone is reported via a highly chemo- and diastereoselective intermolecular Diels-Alder cycloaddition between trans-1,2- disilyloxybenzocyclobutene and the