Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Lou Rocard"'
Autor:
Lou Rocard, Donghuang Chen, Adrien Stadler, Hailong Zhang, Richard Gil, Sophie Bezzenine, Jerome Hannedouche
Publikováno v:
Catalysts, Vol 11, Iss 6, p 674 (2021)
This review summarizes the most noteworthy achievements in the field of C–O and C–N bond formation by hydroalkoxylation and hydroamination reactions on unactivated alkenes (including 1,2- and 1,3-dienes) promoted by earth-abundant 3d transition m
Externí odkaz:
https://doaj.org/article/16b83fcdee80478eacfe98af291c1286
Publikováno v:
Molecules, Vol 25, Iss 6, p 1402 (2020)
Perylenediimide (PDI) is one of the most important classes of dyes and is intensively explored in the field of functional organic materials. The functionalization of this electron-deficient aromatic core is well-known to tune the outstanding optoelec
Externí odkaz:
https://doaj.org/article/f390a5689bbc4db4a101148e9d9e9da2
Autor:
Lou Rocard, Piétrick Hudhomme
Publikováno v:
Catalysts, Vol 9, Iss 3, p 213 (2019)
Palladium-catalyzed cross-coupling reactions are nowadays essential in organic synthesis for the construction of C⁻C, C⁻N, C⁻O, and other C-heteroatom bonds. The 2010 Nobel Prize in Chemistry to Richard F. Heck, Ei-ichi Negishi, and Akira Suzuk
Externí odkaz:
https://doaj.org/article/4daf12ef27444d978f8d242b84c0d48a
Autor:
Aline Makhloutah, Danylo Hatych, Thomas Chartier, Lou Rocard, Antoine Goujon, François-Xavier Felpin, Piétrick Hudhomme
Publikováno v:
Organic & Biomolecular Chemistry. 20:362-365
We report herein an unprecedented palladium-catalyzed cross-coupling reaction between mononitro-perylenediimide (PDI) and various arylstannanes. Optimized conditions developed with this Stille-type reaction allow the grafting of (hetero)aryls of vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b989a80216eb19e5f14139aaf5747bcc
https://doi.org/10.1039/d1ob02291a
https://doi.org/10.1039/d1ob02291a
Autor:
Antoine Goujon, Lou Rocard, Hayley Melville, Thomas Cauchy, Clément Cabanetos, Sylvie Dabos-Seignon, Piétrick Hudhomme
Publikováno v:
Journal of Materials Chemistry C. 10:14939-14945
AzaBenzannulated PeryleneDiimides (AzaBPDIs) and their nitrogen, sulphur and selenium bay-functionalized derivatives are introduced herein as a new class of n-type semiconductors.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ae10ae81a3be0309755c0813e74a3f7
https://doi.org/10.1039/d2tc02999e
https://doi.org/10.1039/d2tc02999e
Small peptides are an ideal class of therapeutics to target protein-protein interactions (PPIs) considering their low toxicity and ability to mimic the large interacting domain of a protein. Nevertheless, they remain underexplored compared to traditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______166::76d0d79e886cc80840988374a1a59574
https://hal.science/hal-03976679
https://hal.science/hal-03976679
Publikováno v:
Chemistry – A European Journal. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0926b0857f9a5b8a7d5e863ac6d9f752
https://doi.org/10.1002/chem.202200519
https://doi.org/10.1002/chem.202200519
Publikováno v:
New Journal of Chemistry. 45:16426-16429
Azido-perylenediimide (N3-PDI) was isolated as a stable solid, which readily converts into N-annulated PDI in solution only when exposed to visible light. N3-PDI was also engaged in CuAAC reactions with alkynes to provide multi-PDI chromophore archit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5544d246279338af13dab8b1f36fc68d
https://doi.org/10.1039/d1nj02130c
https://doi.org/10.1039/d1nj02130c
Publikováno v:
European Journal of Organic Chemistry. 2019:7635-7643
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0558900cf38da254efe6961486db1732
https://doi.org/10.1002/ejoc.201901319
https://doi.org/10.1002/ejoc.201901319
Autor:
Donghuang Chen, Adrien Stadler, Sophie Bezzenine, Jérôme Hannedouche, Hailong Zhang, Lou Rocard, Richard Gil
Publikováno v:
Catalysts
Catalysts, MDPI, 2021, 11 (6), pp.674. ⟨10.3390/catal11060674⟩
Catalysts, Vol 11, Iss 674, p 674 (2021)
Catalysts, MDPI, 2021, 11 (6), pp.674. ⟨10.3390/catal11060674⟩
Catalysts, Vol 11, Iss 674, p 674 (2021)
This review summarizes the most noteworthy achievements in the field of C–O and C–N bond formation by hydroalkoxylation and hydroamination reactions on unactivated alkenes (including 1,2- and 1,3-dienes) promoted by earth-abundant 3d transition m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b970e93a35ba2d6702e91289d5d16f9d
https://hal.archives-ouvertes.fr/hal-03327007/file/catalysts-11-00674-v2.pdf
https://hal.archives-ouvertes.fr/hal-03327007/file/catalysts-11-00674-v2.pdf