Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Youssouf Sanogo"'
Autor:
Boucader Diarra, Modibo Diarra, Oumar Diall, Boubacar Bass, Youssouf Sanogo, Etienne Coulibaly, Mahamadou Sylla, Weining Zhao, Massimo Paone, Giuliano Cecchi
Publikováno v:
Parasites & Vectors, Vol 12, Iss 1, Pp 1-10 (2019)
Abstract Background Tsetse-transmitted trypanosomosis is a deadly, neglected tropical disease and a major challenge for mixed crop-livestock agriculture in sub-Saharan Africa. It is caused by several species of the genus Trypanosoma. Information on t
Externí odkaz:
https://doaj.org/article/e31c1d49b0a14ce995a15eb6601b3db8
Autor:
Julie Febvay, Angela Marinetti, Pascal Retailleau, Arnaud Voituriez, Youssouf Sanogo, Akhila K. Sahoo, Manash Protim Gogoi
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2019, ⟨10.1021/acs.orglett.9b02644⟩
Organic Letters, American Chemical Society, 2019, ⟨10.1021/acs.orglett.9b02644⟩
This study discloses the first enantioselective variant of the gold(I)-catalyzed hydrative cyclizations of ynamides, which have been implemented by using bis-gold(I) complexes of chiral diphosphines. Starting from N-propargyl-ynamides and water in th
Publikováno v:
Chemical Communications
Chemical Communications, Royal Society of Chemistry, 2021, 57 (29), pp.3603-3606. ⟨10.1039/d1cc00081k⟩
Chemical Communications, Royal Society of Chemistry, 2021, 57 (29), pp.3603-3606. ⟨10.1039/d1cc00081k⟩
International audience; Herein, we describe unprecedented access to all-carbon or heterocyclic seven-membered ring frameworks from 1,8-ene-ynes promoted by inexpensive low-valent titanium(II) species, readily available from Ti(OiPr)4 and Grignard rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f97ece7ddc58346d37f26be5ba89ca9
https://hal.archives-ouvertes.fr/hal-03366094
https://hal.archives-ouvertes.fr/hal-03366094
Autor:
Angela Marinetti, Arnaud Voituriez, Xavier Guinchard, Valentin Magné, Youssouf Sanogo, Charles S. Demmer, Pascal Retailleau
Publikováno v:
ACS Catalysis
ACS Catalysis, American Chemical Society, 2020, 10 (15), pp.8141-8148. ⟨10.1021/acscatal.0c01819⟩
ACS Catalysis, American Chemical Society, 2020, ⟨10.1021/acscatal.0c01819⟩
ACS Catalysis, American Chemical Society, 2020, 10 (15), pp.8141-8148. ⟨10.1021/acscatal.0c01819⟩
ACS Catalysis, American Chemical Society, 2020, ⟨10.1021/acscatal.0c01819⟩
International audience; A chiral phosphathiahelicene scaffold displaying a phosphole and a thiophene unit as the terminal rings of the helical sequence has been synthesized and characterized by spectroscopic methods and X-ray diffraction studies. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e6bb896d1ef0a48d8e2642c92cd389d
https://hal.archives-ouvertes.fr/hal-03010211
https://hal.archives-ouvertes.fr/hal-03010211
Autor:
Mahamadou S.M.Sylla, Boucader Diarra, Weining Zhao, Youssouf Sanogo, Giuliano Cecchi, Etienne Coulibaly, Modibo Diarra, Boubacar Bass, Massimo Paone, O. Diall
Publikováno v:
Parasites & Vectors, Vol 12, Iss 1, Pp 1-10 (2019)
Parasites & Vectors
Parasites & Vectors
BackgroundTsetse-transmitted trypanosomosis is a deadly, neglected tropical disease and a major challenge for mixed crop-livestock agriculture in sub-Saharan Africa. It is caused by several species of the genusTrypanosoma. Information on the occurren
Publikováno v:
Chirality
Chirality, Wiley, 2019, 31 (8), pp.561-567. ⟨10.1002/chir.23100⟩
Chirality, Wiley, 2019, 31 (8), pp.561-567. ⟨10.1002/chir.23100⟩
As a complement to our previous studies on the development of a class of chiral phosphahelicenes, this article discloses the synthesis, spectroscopic, and structural characterizations of a new phosphahelicene transition metal complex. It demonstrates
Autor:
Alan Jeuken, Geoffroy Sorin, Mohamed Selkti, Youssouf Sanogo, Janick Ardisson, Raja Ben Othman, Sabrina Dhambri, Joëlle Prunet, Jean-Pierre Férézou, Marie-Isabelle Lannou
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2019, 84 (9), pp.5821-5830. ⟨10.1021/acs.joc.8b03249⟩
Journal of Organic Chemistry, American Chemical Society, 2019, 84 (9), pp.5821-5830. ⟨10.1021/acs.joc.8b03249⟩
A novel approach toward the [5—7]fused bicyclic core of thapsigargin, a subnanomolar inhibitor of the endo/sarcoplasmic calcium ATPase (SERCA), is presented. The synthetic route includes an original Ti(II)-mediated hydroxy-directed reductive coupli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1df22f3cd47dc7dcaa5efcf6848763b3
https://hal.archives-ouvertes.fr/hal-02370403/document
https://hal.archives-ouvertes.fr/hal-02370403/document
Autor:
Luca Allievi, Janick Ardisson, Sabrina Dhambri, Marie-Isabelle Lannou, N. Zeghbib, Camille Lecourt, Geoffroy Sorin, R. Ben Othman, Youssouf Sanogo
Publikováno v:
Natural Product Reports
Natural Product Reports, Royal Society of Chemistry, 2018, 35 (1), pp.105-124. ⟨10.1039/c7np00048k⟩
Natural Product Reports, Royal Society of Chemistry, 2018, 35 (1), pp.105-124. ⟨10.1039/c7np00048k⟩
Covering: 2002 to August 2017. This review highlights recent RCM reactions towards the synthesis of sterically congested natural products. It offers an insight into various synthetic targets and approaches and provides information on the evolution of
Autor:
Franck Ferreira, Youssouf Sanogo, Fabrice Chemla, Valentin N. Bochatay, Olivier Jackowski, Alejandro Perez-Luna
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2015, 357 (13), pp.2809--2814. ⟨10.1002/adsc.201500347⟩
Advanced Synthesis and Catalysis, 2015, 357 (13), pp.2809--2814. ⟨10.1002/adsc.201500347⟩
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2015, 357 (13), pp.2809--2814. ⟨10.1002/adsc.201500347⟩
Advanced Synthesis and Catalysis, 2015, 357 (13), pp.2809--2814. ⟨10.1002/adsc.201500347⟩
International audience
Autor:
Luca Allievi, Sabrina Dhambri, Camille Lecourt, Marie-Isabelle Lannou, Geoffroy Sorin, Janick Ardisson, Youssouf Sanogo
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2016, 72 (24), pp.3369-3377. ⟨10.1016/j.tet.2016.04.005⟩
Tetrahedron, Elsevier, 2016, 72 (24), pp.3369-3377. ⟨10.1016/j.tet.2016.04.005⟩
International audience; This review covers the different syntheses of two sesquiterpenes with unprecedented tetracyclic [3-5-5-7] framework, echinopines A and B. The synthetic strategies and ring-forming sequences are presented with emphasis on the m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa3e413fa91dc6387e2a3f3f0b5e186d
https://hal.archives-ouvertes.fr/hal-02370507
https://hal.archives-ouvertes.fr/hal-02370507