Zobrazeno 1 - 10
of 210
pro vyhledávání: '"Fabrice Chemla"'
Autor:
Angel Palillero-Cisneros, Paola G. Gordillo-Guerra, Fernando García-Alvarez, Olivier Jackowski, Franck Ferreira, Fabrice Chemla, Joel L. Terán, Alejandro Perez-Luna
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 1443-1451 (2023)
We demonstrate that α-(aminomethyl)acrylates are suitable acceptors for 1,4-additions of dialkylzincs in aerobic conditions. The air-promoted radical–polar crossover process involves the 1,4-addition of an alkyl radical followed by homolytic subst
Externí odkaz:
https://doaj.org/article/e8be299227c5484aa98b9cb39ba0fbfe
Autor:
Federico Banchini, Baptiste Leroux, Erwan Le Gall, Marc Presset, Olivier Jackowski, Fabrice Chemla, Alejandro Perez‐Luna
Publikováno v:
Chemistry – A European Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9dc45cb9b905a5df970d5d1887e1753
https://doi.org/10.1002/chem.202301084
https://doi.org/10.1002/chem.202301084
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 236-245 (2013)
The formation of alkylidenezinc carbenoids by 1,4-addition/carbozincation of dialkylzincs or alkyl iodides based on zinc atom radical transfer, in the presence of dimethylzinc with β-(propargyloxy)enoates having pendant iodo- and bromoalkynes, is di
Externí odkaz:
https://doaj.org/article/0443e74070b64ea1bc0ae5c6dc71abe0
Autor:
Johana Ramirez Hernandez, Fabrice Chemla, Franck Ferreira, Olivier Jackowski, Julie Oble, Alejandro Perez-Luna, Giovanni Poli
Publikováno v:
CHIMIA, Vol 70, Iss 1-2 (2016)
The use of tert-butanesulfinamides as nitrogen nucleophiles in carbon–nitrogen bond forming reactions is reviewed. This field has grown in the shadow of the general interest in N-tert-butanesulfinyl imines for asymmetric synthesis and occupies now
Externí odkaz:
https://doaj.org/article/8dda8bb200e4414aa7b4c4b803482a92
Autor:
Franck Ferreira, Karen de la Vega-Hernández, Fabrice Chemla, Alejandro Perez-Luna, Olivier Jackowski
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2021, 23 (11), pp.4426-4430. ⟨10.1021/acs.orglett.1c01367⟩
Organic Letters, American Chemical Society, 2021, 23 (11), pp.4426-4430. ⟨10.1021/acs.orglett.1c01367⟩
International audience; The stereoselective germylzincation of internal alkynes delivering trisubstituted vinylgermanes is achieved via a radical chain process involving Ph3GeH and Et2Zn with AIBN as initiator. Excellent levels of regiocontrol are ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e754bd90ce188be9dd78e158436d166c
https://pubmed.ncbi.nlm.nih.gov/34032457
https://pubmed.ncbi.nlm.nih.gov/34032457
Autor:
S. Yamago, G. M. Sammis, Davide Ravelli, M. Fagnoni, M. P. Sibi, Cheriehan Hessin, S. Protti, K. Mitsudo, H. Subramaniann, J. A. Murphy, Yufeng Ren, D. Dimitrova, Louis Fensterbank, R. A. Ii Flowers, A. Pérez-Luna, Cyril Ollivier, I. Ryu, T. G. Bolduc, J.-P. Goddard, S. Sumino, M. Desage-El Murr, T. Qin, B. Thomson, K. F. Clark, M. Zhou, Y. Lu, T. Fukuyama, Agnideep Das, S. Suga, Fabrice Chemla, M. Cormier, Caroline O. Bartulovich, Z.-Q. Liu, Tesia V. Chciuk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb09eb2f4a7182414545464832dbfadc
https://doi.org/10.1055/b000000086
https://doi.org/10.1055/b000000086
Autor:
D. Liu, T. P. Yoon, C. Melendez, C. Ollivier, E. André-Joyaux, O. Ouari, B. Braïda, Fabrice Chemla, L. Gnägi, F. Dénès, J. Zhang, G. Casano, M. Bietti, A. Serafino, S. Chiba, E. Besson, H. Yorimitsu, V. Soulard, M. P. Bertrand, X.-L. Lu, P. Renaud, Y.-F. Wang, B. Wang, Etienne Derat, S. Lakhdar, T. Rovis, S. Treacy, S. B. Cahoon, F.-L. Zhang, S. Chelli, A. Kaga, C. Bellanger, Louis Fensterbank, X. Zhang, Giovanni Maestri, E. Shirakawa, Y. Chen, S. Gastaldi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b4e03a90942dcd59c40ffb4fab384d4
https://doi.org/10.1055/b000000087
https://doi.org/10.1055/b000000087
Autor:
A. Pérez-Luna, Fabrice Chemla
Publikováno v:
Free Radicals: Fundamentals and Applications in Organic Synthesis 2
Radical–polar crossover reactions, that is, single-electron redox events allowing for the interconversion between radical and ionic intermediates, make it possible to connect radical and polar processes in the same synthetic transformation. Such a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56ea57722ca4f539d80c9003f7d13c1c
https://doi.org/10.1055/sos-sd-233-00075
https://doi.org/10.1055/sos-sd-233-00075
Autor:
Olivier Jackowski, Karen de la Vega-Hernández, Fabrice Chemla, Alejandro Perez-Luna, Franck Ferreira, Kevin Isaac
Publikováno v:
Helvetica Chimica Acta
Helvetica Chimica Acta, Wiley, In press, ⟨10.1002/hlca.202100128⟩
Helvetica Chimica Acta, Wiley, In press, ⟨10.1002/hlca.202100128⟩
International audience; The silyl-and germylzincation of terminal or internal propargylic alcohols by reaction with (Me3Si)3SiH/Et2Zn, [(Me3Si)3Si]2Zn/Et2Zn or Ph3GeH/Et2Zn is examined. These reactions proceed through the addition of silicon-or germa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50b8db64b5c76888d4579c2d2b9988bb
https://hal.sorbonne-universite.fr/hal-03356128
https://hal.sorbonne-universite.fr/hal-03356128
Autor:
Fabrice Chemla, Karen de la Vega-Hernández, Hélène Gérard, Martin Oestreich, Juan Sanz García, Stéphanie Halbert, Alejandro Perez-Luna, Carolin Fopp, Olivier Jackowski, Frédéric Guégan, Franck Ferreira, Elise Romain
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2021, 363 (10), pp.2634-2647. ⟨10.1002/adsc.202001566⟩
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2021, 363 (10), pp.2634-2647. ⟨10.1002/adsc.202001566⟩
International audience; Aryl- and hetaryl-substituted acetylenes undergo regio- and stereoselective silylzincation by reaction with [(Me3Si)3Si]2Zn in the presence of Et2Zn (10–110 mol%) as additive. The distinctive feature of this addition across
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7149f4d835e21a2f8b9d16e43c576174
https://hal.sorbonne-universite.fr/hal-03236531/document
https://hal.sorbonne-universite.fr/hal-03236531/document