Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Manuel Barday"'
Autor:
Manuel Barday, Jessica Rodrigues, Pierre Bouillac, Jean Rodriguez, Muriel Amatore, Thierry Constantieux
Publikováno v:
Advanced Synthesis & Catalysis. 365:148-155
Autor:
Jingyang Qin, Manuel Barday, Samikshan Jana, Nil Sanosa, Ignacio Funes-Ardoiz, Christopher Teskey
The development of methods to form C–C bonds from readily-available starting materials is essential in driving innovation of functional molecules. In this context, hydrofunctionalisation of feedstock alkenes via catalytic hydrogen atom transfer fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0af9eba642503ee5fbc8d6fa9e5a3fb2
https://doi.org/10.26434/chemrxiv-2023-3rshq
https://doi.org/10.26434/chemrxiv-2023-3rshq
Autor:
Christophe Aïssa, Eva Nicolas, Manuel Barday, Francois Delmotte, Bradley Higginson, Martin Appelmans
Publikováno v:
SYNTHESIS-STUTTGART
Controlling the behavior of terminal alkynes in metal-catalyzed intermolecular tandem reactions is a formidable challenge despite the potential advantage offered by these strategies in modern synthesis. Herein, we describe that a nickel catalyst enab
Autor:
Pierre Bouillac, Yoann Coquerel, Manuel Barday, Muriel Amatore, Jean Rodriguez, Thierry Constantieux
Publikováno v:
European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2021, 2021 (21), pp.3023-3034. ⟨10.1002/ejoc.202100405⟩
European Journal of Organic Chemistry, 2021, 2021 (21), pp.3023-3034. ⟨10.1002/ejoc.202100405⟩
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2021, 2021 (21), pp.3023-3034. ⟨10.1002/ejoc.202100405⟩
European Journal of Organic Chemistry, 2021, 2021 (21), pp.3023-3034. ⟨10.1002/ejoc.202100405⟩
International audience; The progress in enantioselective organocatalysis have enabled efficient and highly stereoselective syntheses of cyclobutane derivatives, through (2 + 2) annulation reactions, overcoming the geometrical constraints inherent to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10515a26c033efc25c6530160ed6c29f
https://hal.archives-ouvertes.fr/hal-03370300
https://hal.archives-ouvertes.fr/hal-03370300
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2020, pp.131153. ⟨10.1016/j.tet.2020.131153⟩
Tetrahedron, 2020, pp.131153. ⟨10.1016/j.tet.2020.131153⟩
Tetrahedron, Elsevier, 2020, pp.131153. ⟨10.1016/j.tet.2020.131153⟩
Tetrahedron, 2020, pp.131153. ⟨10.1016/j.tet.2020.131153⟩
International audience; An unprecedented remote and regioselective trifluoromethylthiolation reaction of alcohols was developed. Under mild conditions, a panel of free-alcohols was selectively functionalized with TolSO2SCF3 reagent as the SCF3 source
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bceaa4f7b8967e075b52a9ae3e41dda4
https://hal.archives-ouvertes.fr/hal-02567996
https://hal.archives-ouvertes.fr/hal-02567996
Autor:
Christopher Janot, Bradley Higginson, Christophe Aïssa, Kelvin Y. T. Ho, Daniel Clare, Caitlin Carr-Knox, Manuel Barday
Publikováno v:
SYNTHESIS-STUTTGART
The study of the regioselectivity of insertion of unsymmetrical alkynes into the carbon–carbon bond of oxetan-3-one in the presence of a nickel catalyst has revealed a strong directing effect of a 2-thienyl substituent. This effect is larger than t
Autor:
Manuel Barday, Nathan R. Halcovitch, Christopher Janot, James Campbell Muir, Christophe Aïssa
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie
Angewandte Chemie
The functionalization of carbon-hydrogen bonds in non-nucleophilic substrates using α-carbonyl sulfoxonium ylides has not been so far investigated, despite the potential safety advantages that such reagents would provide over either diazo compounds
Autor:
Austin L. Burman, Manuel Barday, Mitchell R. Ashkin, Thomas G. Back, Belinda Heyne, Thomas C. Malig
Carvedilol is a widely prescribed drug for the treatment of heart failure and the prevention of associated ventricular arrhythmias. It has also been reported to function as a biological antioxidant via hydrogen atom transfer from its carbazole N–H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb25f04cb60e5a25fbc3290eeeb9b07e
https://europepmc.org/articles/PMC6071783/
https://europepmc.org/articles/PMC6071783/
Publikováno v:
ChemInform. 47
1,3-enynes are convenient surrogates of internal alkynes bearing two alkyl substituents in their nickel-catalyzed [4 + 2] cycloaddition with 3-azetidinones.