Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Gilles, Hanquet"'
Autor:
Clément Delobel, Armen Panossian, Gilles Hanquet, Frédéric R. Leroux, Fabien Toulgoat, Thierry Billard
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 2434-2441 (2024)
Trifluoromethoxylated molecules and selenylated compounds find a wide range of interesting applications, but separately. In order to combine the potential of these two motifs and to propose a new class of compounds, we have developed an electrophilic
Externí odkaz:
https://doaj.org/article/3693e32906304638ba0b4460d653f254
Autor:
Andrej Emanuel Cotman, Thomas Guérin, Ivana Kovačević, Davide Benedetto Tiz, Martina Durcik, Federica Fulgheri, Štefan Možina, Daniela Secci, Maša Sterle, Janez Ilaš, Anamarija Zega, Nace Zidar, Lucija Peterlin Mašič, Tihomir Tomašič, Frédéric R. Leroux, Gilles Hanquet, Danijel Kikelj
Publikováno v:
ACS Omega, Vol 6, Iss 14, Pp 9723-9730 (2021)
Externí odkaz:
https://doaj.org/article/9ba5d039df7149c1b22ceb9e931835a8
Autor:
Sergii Pazenok, David Bernier, Morgan Donnard, Gilles Hanquet, Armen Panossian, Frédéric R. Leroux
Publikováno v:
PATAI'S Chemistry of Functional Groups. :1-77
Autor:
Anaïs Loison, Gilles Hanquet, Fabien Toulgoat, Thierry Billard, Armen Panossian, Frédéric R. Leroux
Publikováno v:
Organic Letters. 24:8316-8321
We report herein the
Autor:
Emilie Evain-Bana, Lucie Schiavo, Christophe Bour, Don Antoine Lanfranchi, Simone Berardozzi, Francesca Ghirga, Denyse Bagrel, Bruno Botta, Gilles Hanquet, Mattia Mori
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 113-118 (2017)
The cell division cycle 25 phosphatases (CDC25A, B, and C; E.C. 3.1.3.48) are key regulator of the cell cycle in human cells. Their aberrant expression has been associated with the insurgence and development of various types of cancer, and with a poo
Externí odkaz:
https://doaj.org/article/9849d8058a8e460d947b419399a0e753
Publikováno v:
Angewandte Chemie (International ed. in English).
The deprotonative functionalization of α,α-difluoromethyl ketones is described herein. Using a catalytic organosuperbase and a silane additive, the corresponding difluoroenolate could be generated and trapped with aldehydes to deliver various α,α
Autor:
Armen Panosian, Thierry Billard, Clémence Bonnefoy, Fabien Toulgoat, Emmanuel Chefdeville, Gilles Hanquet, Frédéric R. Leroux
Publikováno v:
Chemistry – A European Journal. 27:15986-15991
Despite recent advances, trifluoromethoxylation remains a challenging reaction. Here we describe an efficient trifluoromethoxylative substitution, using an inexpensive and easy-to-handle reagent. By mixing DMAP with a slight excess of 1,4-dinitro-tri
Autor:
Clémence Bonnefoy, Emmanuel Chefdeville, Christian Tourvieille, Armen Panossian, Gilles Hanquet, Frédéric Leroux, Fabien Toulgoat, Thierry Billard
Publikováno v:
Chemistry – A European Journal. 28
Autor:
Clémence Bonnefoy, Emmanuel Chefdeville, Christian Tourvieille, Armen Panossian, Gilles Hanquet, Frédéric Leroux, Fabien Toulgoat, Thierry Billard
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, 2022, 28 (43), ⟨10.1002/chem.202201589⟩
Chemistry-A European Journal, 2022, 28 (43), ⟨10.1002/chem.202201589⟩
International audience; Carbamoyl fluoride is a fluorinated group which, to this date, remains underexplored, probably due to the lack of data concerning their properties. In this paper, a study of carbamoyl fluoride is proposed. Stability studies, i
Autor:
Frédéric R. Leroux, Maša Sterle, Janez Ilaš, Thomas Guérin, Martina Durcik, Lucija Peterlin Mašič, Daniela Secci, Gilles Hanquet, Davide Benedetto Tiz, Tihomir Tomašič, Andrej Emanuel Cotman, Nace Zidar, Federica Fulgheri, Štefan Možina, Ivana Kovačević, Anamarija Zega, Danijel Kikelj
Publikováno v:
ACS Omega, Vol 6, Iss 14, Pp 9723-9730 (2021)
ACS Omega
ACS Omega, ACS Publications, 2021, 6 (14), pp.9723-9730. ⟨10.1021/acsomega.1c00331⟩
ACS Omega
ACS Omega, ACS Publications, 2021, 6 (14), pp.9723-9730. ⟨10.1021/acsomega.1c00331⟩
International audience; A practical access to four new halogen-substituted pyrrole building blocks was realized in two to five synthetic steps from commercially available starting materials. The target compounds were prepared on a 50 mg to 1 g scale,