Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Anne-Lise Dhimane"'
Publikováno v:
Electroorganic Synthesis ISBN: 9780203758571
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f47eb24211a567294d7ee4fc50ebaa4
https://doi.org/10.1201/9780203758571-27
https://doi.org/10.1201/9780203758571-27
Autor:
Etienne Levernier, Alex Cartier, Takahide Fukuyama, Anne-Lise Dhimane, Louis Fensterbank, Ilhyong Ryu, Cyril Ollivier
Publikováno v:
Advanced Synthesis & Catalysis. 362:2254-2259
Autor:
Etienne Levernier, Takahide Fukuyama, Cyril Ollivier, Ilhyong Ryu, Vincent Corcé, Louis Fensterbank, Alex Cartier, Anne-Lise Dhimane
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2019, 58 (6), pp.1789-1793. ⟨10.1002/ange.201811858⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2019, 58 (6), pp.1789-1793. ⟨10.1002/ange.201811858⟩
International audience; Primary, secondary and tertiary alkyl radicals, formed by photocatalyzed oxidation of organosilicates, can be involved efficiently in radical carbonylation with carbon monoxide (CO), which leads to a variety of unsymmetrical k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a01e2d7bbfd85bd5c8f177d796d3931
https://hal.sorbonne-universite.fr/hal-02010150/document
https://hal.sorbonne-universite.fr/hal-02010150/document
Autor:
Louis Fensterbank, Anne-Lise Dhimane, Takahide Fukuyama, Kazusa Miyagawa, Célia Brancour, Yuko Ohta, Max Malacria, Ilhyong Ryu
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2012, 18 (23), pp.7243-7247. ⟨10.1002/chem.201200045⟩
Chemistry-A European Journal, 2012, 18 (23), pp.7243-7247. ⟨10.1002/chem.201200045⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2012, 18 (23), pp.7243-7247. ⟨10.1002/chem.201200045⟩
Chemistry-A European Journal, 2012, 18 (23), pp.7243-7247. ⟨10.1002/chem.201200045⟩
International audience; We have developed novel Rh-catalyzed [n+1]-type cycloadditions of 1,4-enyne esters, which involve an acyloxy migration as a key step. The efficient preparation of functionalized resorcinols, including biaryl derivatives, from
Publikováno v:
European Journal of Organic Chemistry. 2009:1674-1678
A straightforward and unprecedented method towards the synthesis of 3-silapiperidines is described. The key step involves a formal double nucleophilic substitution reaction between the (bromomethyl)dimethylsilyl chloride and a N,C-sp2-1,4-dianionic s
Autor:
Gilles Lemière, Alexandra Hours, Takahide Fukuyama, Louis Fensterbank, Max Malacria, Anne-Lise Dhimane, Vincent Gandon, Kevin Cariou
Publikováno v:
Journal of the American Chemical Society. 131:2993-3006
Cyclopentenylidene gold complexes can easily be formed from vinyl allenes through a Nazarov-like mechanism. Such carbenes may transform in four different ways into polycyclic frameworks: electrophilic cyclopropanation, C-H insertion, C-C migration, o
Autor:
Nicolas Puljic, Paola Carta, Max Malacria, Carine Robert, Anne-Lise Dhimane, Cyril Ollivier, Emmanuel Lacôte, Louis Fensterbank
Publikováno v:
Tetrahedron. 64:11865-11875
Two efficient procedures involving tin hydride or thiophenol-mediated intramolecular homolytic substitution at the sulfur atom are reported. They lead to the generation of varied P(V)-centered radicals from the corresponding aryl or alkyne thiophosph
Transannular Radical Cascade as an Approach to the Diastereoselective Synthesis of Linear Triquinane
Publikováno v:
Angewandte Chemie International Edition. 41:3284-3287
Publikováno v:
Pure and Applied Chemistry. 72:1605-1613
This article reviews our contribution in the field of radical synthetic chemistry, focusing on cascades relying on the use of propargylic BMDMS ethers and asymmetric synthesis using enantiopure vinylsulfoxides.
Publikováno v:
European Journal of Organic Chemistry. 2000:155-163
Two strategies have been explored to build the highly strained eleven-membered ring 2, a potential precursor for the biosynthetic key intermediate of the protoilludane family: an intramolecular Horner-Wadsworth-Emmons olefination and an intramolecula