Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Bertrand Lede"'
Autor:
Bertrand Lede, Nathalie Van Hijfte, Benoît Rigo, Alina Ghinet, Adam Daïch, Jean‐Pierre Henichart, Ulrich Darbost, Philippe Gautret, Elena Bîcu
Publikováno v:
ChemInform. 46
The π-cationic arylation of methoxy substituted benzoic acids with reactive arenes [e.g. (II)] is developed to provide an optimized synthetic route to phenstatin (V).
Autor:
Alina Ghinet, Adam Daïch, Ulrich Darbost, Nathalie Van Hijfte, Benoît Rigo, Bertrand Lede, Jean‐Pierre Henichart, Philippe Gautret, Elena Bîcu
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2014, 20 (32), pp.10117-10130. ⟨10.1002/chem.201402377⟩
Chemistry-A European Journal, 2014, 20 (32), pp.10117-10130. ⟨10.1002/chem.201402377⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2014, 20 (32), pp.10117-10130. ⟨10.1002/chem.201402377⟩
Chemistry-A European Journal, 2014, 20 (32), pp.10117-10130. ⟨10.1002/chem.201402377⟩
International audience; A rapid domino π-cationic arylation of aromatic carboxylic acids, mediated by Eaton's reagent, has been developed for the synthesis of Iasi-red polymethoxylated polycyclic aromatic hydrocarbons (PAHs). This route is currently
Autor:
Flavien Vincent, MD, PhD, Bertrand Ledermann, MD, Jean-Etienne Ricci, MD, Guillaume Cayla, MD, PhD, Benoit Lattuca, MD, PhD
Publikováno v:
JACC: Case Reports, Vol 2, Iss 15, Pp 2411-2413 (2020)
Pathological studies have revealed spontaneous recanalized coronary thrombi as a frequent evolution of coronary occlusions; however, they are poorly recognized on coronary angiography, and the optimal therapeutic strategy for clinical evolution is un
Externí odkaz:
https://doaj.org/article/34676d6971ad4d9ca0d9772d74ae3061