Zobrazeno 1 - 10
of 230
pro vyhledávání: '"Gwilherm Evano"'
Autor:
Clément Jacob, Hajar Baguia, Amaury Dubart, Samuel Oger, Pierre Thilmany, Jérôme Beaudelot, Christopher Deldaele, Stefano Peruško, Yohann Landrain, Bastien Michelet, Samuel Neale, Eugénie Romero, Cécile Moucheron, Veronique Van Speybroeck, Cédric Theunissen, Gwilherm Evano
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-8 (2022)
The construction of four-membered rings via a 4-exo-dig cyclization was originally theorized to be unfavourable and only recently shown in sparse examples. Here the authors present a photochemical, radical 4-exo-dig cyclization of ynamides to form az
Externí odkaz:
https://doaj.org/article/74a30cbf227b4922802fd7718b8ea522
Autor:
Pierre Thilmany, Alejandro Guarnieri-Ibáñez, Clément Jacob, Jérôme Lacour, Gwilherm Evano
Publikováno v:
ACS Organic & Inorganic Au, Vol 2, Iss 1, Pp 53-58 (2021)
Externí odkaz:
https://doaj.org/article/100abeaff84d4a1a9058f9b319c384ec
Autor:
Samuel Oger, Hajar Baguia, Tuan-Anh Phan, Titouan Teunens, Jérôme Beaudelot, Cécile Moucheron, Gwilherm Evano
Publikováno v:
SynOpen, Vol 05, Iss 02, Pp 141-144 (2021)
Externí odkaz:
https://doaj.org/article/ef78563d29f244149b40043ab96959fc
Autor:
Benoit Métayer, Andrea Angeli, Agnès Mingot, Kévin Jouvin, Gwilherm Evano, Claudiu T. Supuran, Sébastien Thibaudeau
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 33, Iss 1, Pp 804-808 (2018)
After hydrofluorination of ynesulphonamides in superacid or in the presence of hydrofluoric acid/base reagents, a series of α-fluoroenamides has been synthesised and tested for the inhibition of carbonic anhydrase (CA, EC 4.2.1.1) isoforms. This stu
Externí odkaz:
https://doaj.org/article/3e5fde0bdc51425db5d7f1f930503f06
Autor:
Christopher Deldaele, Bastien Michelet, Hajar Baguia, Sofia Kajouj, Eugenie Romero, Cecile Moucheron, Gwilherm Evano
Publikováno v:
CHIMIA, Vol 72, Iss 9 (2018)
Organic transformations can broadly be classified into four categories including cationic, anionic, pericyclic and radical reactions. While the last category has been known for decades to provide remarkably efficient synthetic pathways, it has long b
Externí odkaz:
https://doaj.org/article/20ec60fa53c44d8699e57ad9d265853a
Publikováno v:
Frontiers in Chemistry, Vol 6 (2018)
Halogenated arenes and alkenes are of prime importance in many areas of science, especially in the pharmaceutical, agrochemical, and chemical industries. While the simplest ones are commercially available, some of them are still hardly accessible dep
Externí odkaz:
https://doaj.org/article/bc039f8a4c6543c1bdc0afad944002a0
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 2214-2222 (2012)
We have developed a general synthesis of polysubstituted 1,4-dihydropyridines and pyridines based on a highly regioselective lithiation/6-endo-dig intramolecular carbolithiation from readily available N-allyl-ynamides. This reaction, which has been s
Externí odkaz:
https://doaj.org/article/06ea34a2e9fd438687a3bc78cc20cb00
Autor:
Mangaleswaran Sivaprakasham, François Couty, Gwilherm Evano, B. Srinivas, R. Sridhar, K. Rama Rao
Publikováno v:
ARKIVOC, Vol 2007, Iss 10, Pp 71-93 (2006)
Externí odkaz:
https://doaj.org/article/003624c00faa40bca79eb5d0bca6753d
Publikováno v:
Synthesis. 55:1799-1823
Anilines selectively arylated at their ortho, meta or para positions are useful building blocks in synthesis and have found applications in many areas. The most straightforward method for their synthesis relies on the direct arylation of a C(sp2)–H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::082dd4e2cfcbef1e90d2cae5ba69f69b
https://doi.org/10.1055/a-2039-7985
https://doi.org/10.1055/a-2039-7985
Publikováno v:
Synthesis. 55:272-288
An efficient radical cyclization of suitably functionalized ynamides to nitrogen-containing heterocycles is reported. Upon reaction with tributyltin hydride in the presence of catalytic amounts of AIBN in toluene at 80 °C, a range of ynamides bearin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::501e79f176a5431ea86c55954015927b
https://doi.org/10.1055/a-1868-8092
https://doi.org/10.1055/a-1868-8092