Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Marie Vayer"'
Publikováno v:
Chemical Communications. 59:6231-6234
A new class of self-assembled bidentate NDI-derived ligands featuring π–π interactions is described, which were successfully used in rhodium-catalyzed enantioselective hydrogenation of diverse olefins.
Publikováno v:
Chemical Science. 14:2983-2989
The use of epoxides as aldehyde surrogates allows isochromans to be constructed with greater scope than previously reported oxa-Pictet–Spengler reactions. The initial Meinwald rearrangement and subsequent steps are promoted by HFIP and triflic acid
Publikováno v:
ACS Catalysis. 12:10995-11001
Publikováno v:
ACS Catalysis
ACS Catalysis, 2022, 12 (6), pp.3309-3316. ⟨10.1021/acscatal.2c00216⟩
ACS Catalysis, 2022, 12 (6), pp.3309-3316. ⟨10.1021/acscatal.2c00216⟩
The reduction of epoxides is a powerful tool to access anti-Markovnikov alcohols, but reported methods are poorly compatible with strongly electronically deactivated substrates. Here, we describe a general method for the linear-selective reduction of
Publikováno v:
Angewandte Chemie. 135
β-Arylethylamines are prevalent structural motifs in molecules exhibiting biological activity. Here we report a sequential one-pot protocol for the 1,2-aminoarylation of alkenes with hydroxylammonium triflate salts and (hetero)arenes. Unlike existin
Autor:
Tommaso Bortolato, Gianluca Simionato, Marie Vayer, Cristian Rosso, Lorenzo Paoloni, Edmondo M. Benetti, Andrea Sartorel, David Lebœuf, Luca Dell’Amico
Photocatalysis has become a prominent tool in the arsenal of organic chemists to develop and (re)imagine transformations. However, only a handful of versatile organic photocatalysts (PCs) are available, hampering the discovery of new reactivities. He
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e67f90c3da497e826a4adfb8366eda70
https://hdl.handle.net/11577/3466221
https://hdl.handle.net/11577/3466221
Autor:
Marie Vayer, Sophie Rodrigues, Solène Miaskiewicz, David Gatineau, Yves Gimbert, Vincent Gandon, Christophe Bour
Publikováno v:
ACS Catalysis. 12:305-315
Autor:
Andrei Golushko, Florent Noël, Shaofei Zhang, Marie Vayer, Nazanin Rezajooei, Christopher N. Rowley, Vuk D. Vuković, Joseph Moran, David Lebœuf
Publikováno v:
Chem
Chem, Cell Press, In press, ⟨10.1016/j.chempr.2021.10.023⟩
Chem, In press, ⟨10.1016/j.chempr.2021.10.023⟩
Chem, Cell Press, In press, ⟨10.1016/j.chempr.2021.10.023⟩
Chem, In press, ⟨10.1016/j.chempr.2021.10.023⟩
International audience; Alcohols and epoxides are arguably ideal electrophiles for the Friedel-Crafts alkylation, since they are widely available, require no pre-activation, and produce no stoichiometric waste beyond water. However, neither primary a
Autor:
Refka Guermazi, Christophe Bour, Yan Chen, Régis Guillot, Jiaxin Tian, Alexandre Djurovic, Vincent Gandon, Samuel Dagorne, Marie Vayer
Publikováno v:
Chemistry – A European Journal. 26:12831-12838
The catalytic activity of cationic NHC-ZnII and NHC-AlIII (NHC=N-heterocyclic carbene) complexes in reactions that require the electrophilic activation of soft C-C π bonds has been studied. The former proved able to act as a soft π-Lewis acid in a
Publikováno v:
European Journal of Organic Chemistry. 2020:5350-5357