Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Olivier Basle"'
Autor:
Juliette Zanzi, Zachary Pastorel, Carine Duhayon, Elise Lognon, Christophe Coudret, Antonio Monari, Isabelle M. Dixon, Yves Canac, Michael Smietana, Olivier Baslé
Publikováno v:
JACS Au, Vol 4, Iss 8, Pp 3049-3057 (2024)
Externí odkaz:
https://doaj.org/article/ced2509263bf4bca8f5c037da6ff6cb9
Publikováno v:
L'Actualité Chimique
L'Actualité Chimique, Société chimique de France, 2018, pp.18-28
L'Actualité Chimique, 2018, 432, pp.18-28
HAL
L'Actualité Chimique, Société chimique de France, 2018, pp.18-28
L'Actualité Chimique, 2018, 432, pp.18-28
HAL
National audience; With the ineluctable rarefaction of fossil resources, the production of biosourced synthetic building-blocks from renewable raw materials has become one of the major challenges of the 21st century. To this concern, the olefin metat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::61c4625a0d7522d7e86e25ee089fbb89
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01905112
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01905112
Autor:
Olivier Basle, et al. et al.
Publikováno v:
ChemInform. 45
Autor:
Pierre Queval, Mathieu Rouen, Annie-Claude Gaumont, Isabelle Dez, Olivier BASLE, Marc Mauduit
Publikováno v:
Olefin Metathesis: Theory and Practice
Karol Grela. Olefin Metathesis: Theory and Practice, Wiley, Chapter 10, 2013, 978-1-118-20794-9
HAL
Karol Grela. Olefin Metathesis: Theory and Practice, Wiley, Chapter 10, 2013, 978-1-118-20794-9
HAL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::09880b77131fe801c52ee05b31702ff7
https://hal.archives-ouvertes.fr/hal-00881648
https://hal.archives-ouvertes.fr/hal-00881648
Autor:
Olivier Basle, Jean Rodriguez, Anouk Gaudel-Siri, Thierry Constantieux, Jean-Christophe Plaquevent, Maria del Mar Sanchez Duque, Yves Genisson, Nicolas Isambert
Publikováno v:
ChemInform. 42
The novel organocatalytic reaction of cyclic α-substituted β-ketoamides to methyl- or ethylvinylketone proceeds with high yields and enantioselectivities to afford the products bearing all-carbon quaternary stereocenter [cf.
Publikováno v:
ChemInform. 42
Autor:
Olivier Basle, Maria del Mar Sanchez Duque, Damien Bonne, Wilfried Raimondi, Jean Rodriguez, Thierry Constantieux
Publikováno v:
ChemInform. 42
The method furnishes Michael adducts with high anti selectivity (
Autor:
Yves Genisson, Nicolas Isambert, Maria del Mar Sanchez Duque, Jean Rodriguez, Anouk Gaudel-Siri, Thierry Constantieux, Jean-Christophe Plaquevent, Olivier Basle
Publikováno v:
Organic Letters
Organic Letters, 2011, 13, pp.3296. ⟨10.1021/ol200924e⟩
Organic Letters, American Chemical Society, 2011, 13, pp.3296-3299. ⟨10.1021/ol200924e⟩
Organic Letters, American Chemical Society, 2011, 13, pp.3296. ⟨10.1021/ol200924e⟩
Organic Letters, 2011, 13, pp.3296. ⟨10.1021/ol200924e⟩
Organic Letters, American Chemical Society, 2011, 13, pp.3296-3299. ⟨10.1021/ol200924e⟩
Organic Letters, American Chemical Society, 2011, 13, pp.3296. ⟨10.1021/ol200924e⟩
International audience; The secondary amido group of α-substituted β-ketoamides plays a crucial role in the control of the reactivity and spatial arrangement (selectivity) in the organocatalyzed Michael addition to unsaturated carbonyls. This resul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0c61cb55709e353c211521f944b43ed
https://hal.science/hal-01407713
https://hal.science/hal-01407713
Autor:
Wilfried Raimondi, Damien Bonne, Maria del Mar Sanchez Duque, Jean Rodriguez, Olivier Basle, Thierry Constantieux
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2010, 12, pp.5246-5249. ⟨10.1021/ol102289g⟩
Organic Letters, 2010, 12, pp.5246-5249. ⟨10.1021/ol102289g⟩
Organic Letters, American Chemical Society, 2010, 12, pp.5246-5249. ⟨10.1021/ol102289g⟩
Organic Letters, 2010, 12, pp.5246-5249. ⟨10.1021/ol102289g⟩
International audience; The first organocatalytic enantio- and diastereoselective conjugate addition of r-ketoamides to nitroalkenes has been achieved using a bifunctional amino thiourea catalyst. In this new approach, the substrate amide proton play
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9dd884c0faf9e9a6f44848baaaf8e5b
https://hal.archives-ouvertes.fr/hal-00680497
https://hal.archives-ouvertes.fr/hal-00680497
Autor:
Anouk Gaudel-Siri, Jean-Christophe Plaquevent, Yves Genisson, Thierry Constantieux, Olivier Basle, Nicolas Isambert, Jean Rodriguez, M. del Mar Sanchez Duque
Publikováno v:
Synfacts. 2011:0904-0904