Zobrazeno 1 - 10
of 135
pro vyhledávání: '"Hervé Clavier"'
Autor:
César A. Urbina-Blanco, Xavier Bantreil, Hervé Clavier, Alexandra M. Z. Slawin, Steven P. Nolan
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, Pp 1120-1126 (2010)
The steric and electronic influence of backbone substitution in IMes-based (IMes = 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene) N-heterocyclic carbenes (NHC) was probed by synthesizing the [RhCl(CO)2(NHC)] series of complexes to quantify experim
Externí odkaz:
https://doaj.org/article/383cbc63081d4abbb4426428feb97389
Autor:
Jennifer Morvan, Dylan Bouëtard, Lingyu Kong, Yajie Chou, Thomas Vives, Muriel Albalat, Thierry Roisnel, Christophe Crévisy, Paola Nava, Stéphane Humbel, Nicolas Vanthuyne, Hervé Clavier, Marc Mauduit
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, 2023, pp.e202300341. ⟨10.1002/chem.202300341⟩
Chemistry-A European Journal, 2023, pp.e202300341. ⟨10.1002/chem.202300341⟩
International audience; A set of 16 chiral ruthenium complexes containing atropisomerically stable N-Heterocyclic Carbene (NHC) ligands was synthesized from prochiral NHC precursors. After a rapid screening in asymmetric ring-opening-cross metathesis
Autor:
Lingyu Kong, Yajie Chou, Muriel ALBALAT, Marion Jean, Nicolas Vanthuyne, Paola Nava, Stéphane Humbel, Hervé Clavier
Publikováno v:
Dalton Transactions
Dalton Transactions, 2023, 52 (25), pp.8728-8736. ⟨10.1039/d3dt01182h⟩
Dalton Transactions, 2023, 52 (25), pp.8728-8736. ⟨10.1039/d3dt01182h⟩
International audience; The concept of atropisomeric N-heterocyclic carbene (NHC)–metal complexes was extended to NHCs possessing a C2-symmetry and implemented to prepare palladium-based complexes. An in-depth study of the NHC precursors and the sc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9237cabfd45393f4c241edf958981a76
https://hal.science/hal-04142950
https://hal.science/hal-04142950
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, 2022, 364 (4), pp.831-837. ⟨10.1002/adsc.202101099⟩
Advanced Synthesis and Catalysis, 2022, 364 (4), pp.831-837. ⟨10.1002/adsc.202101099⟩
International audience
Autor:
Jennifer Morvan, Dylan Bouëtard, Lingyu Kong, Yajie Chou, Thomas Vives, Muriel Albalat, Thierry Roisnel, Christophe Crévisy, Paola Nava, Stéphane Humbel, Nicolas Vanthuyne, Hervé Clavier, Marc Mauduit
Optically pure ruthenium complexes containing atropisomerically stable N-Heterocyclic Carbene (NHC) ligands are described. Isolated in excellent optical purities (up >99.5% ee) by a successful preparative HPLC resolution on a chiral stationary phase,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8105da84020fd9a0de5c905159f6cbe4
https://doi.org/10.26434/chemrxiv-2022-95shq
https://doi.org/10.26434/chemrxiv-2022-95shq
Autor:
Paola Nava, Stéphane Humbel, Hervé Clavier, Mariia Savchuk, Nicolas Vanthuyne, Damien Hérault, Lucas Bocquin, Muriel Albalat, Marion Jean
Publikováno v:
Chirality
Chirality, Wiley, 2022, 34 (1), pp.13-26. ⟨10.1002/chir.23378⟩
Chirality, 2022, 34 (1), pp.13-26. ⟨10.1002/chir.23378⟩
Chirality, Wiley, 2022, 34 (1), pp.13-26. ⟨10.1002/chir.23378⟩
Chirality, 2022, 34 (1), pp.13-26. ⟨10.1002/chir.23378⟩
International audience; From achiral imidazolinium salts, chiral transition metal complexes containing an N-heterocyclic carbene (NHC) ligand were prepared (metal = palladium, copper, silver, gold, rhodium). Axial chirality in these complexes results
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f84b5254971bd5afaa74e5f8373eea3
https://hal.archives-ouvertes.fr/hal-03500191
https://hal.archives-ouvertes.fr/hal-03500191
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2021, 363 (10), pp.2578-2585. ⟨10.1002/adsc.202001575⟩
Advanced Synthesis and Catalysis, 2021, 363 (10), pp.2578-2585. ⟨10.1002/adsc.202001575⟩
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2021, 363 (10), pp.2578-2585. ⟨10.1002/adsc.202001575⟩
Advanced Synthesis and Catalysis, 2021, 363 (10), pp.2578-2585. ⟨10.1002/adsc.202001575⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05c65e46d32b7687972d1c34b676b2b6
https://hal.archives-ouvertes.fr/hal-03273319/document
https://hal.archives-ouvertes.fr/hal-03273319/document
C 1 ‐Symmetric Atropisomeric NHC Palladium(II) Complexes: Synthesis, Resolution and Characterization
Autor:
Stéphane Humbel, Hervé Clavier, Marion Jean, Lingyu Kong, Nicolas Vanthuyne, Muriel Albalat, Paola Nava, Yajie Chou
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2021, 363 (17), pp.4229-4238. ⟨10.1002/adsc.202100491⟩
Advanced Synthesis and Catalysis, 2021, 363 (17), pp.4229-4238. ⟨10.1002/adsc.202100491⟩
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2021, 363 (17), pp.4229-4238. ⟨10.1002/adsc.202100491⟩
Advanced Synthesis and Catalysis, 2021, 363 (17), pp.4229-4238. ⟨10.1002/adsc.202100491⟩
International audience; Series of chiral palladium(II) allyl and cinnamyl complexes bearing a C1-symmetric N-heterocyclic carbenes were synthesized from achiral precursors. The chirality of theses complexes results from the formation of the carbene-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c6d3d3bf42be755e8259a7f4a6ccfb4
https://hal.archives-ouvertes.fr/hal-03338494/document
https://hal.archives-ouvertes.fr/hal-03338494/document
Publikováno v:
Journal of Physical Chemistry A
Journal of Physical Chemistry A, American Chemical Society, 2020, 124 (42), pp.8753-8765. ⟨10.1021/acs.jpca.0c06746⟩
Journal of Physical Chemistry A, 2020, 124 (42), pp.8753-8765. ⟨10.1021/acs.jpca.0c06746⟩
Journal of Physical Chemistry A, American Chemical Society, 2020, 124 (42), pp.8753-8765. ⟨10.1021/acs.jpca.0c06746⟩
Journal of Physical Chemistry A, 2020, 124 (42), pp.8753-8765. ⟨10.1021/acs.jpca.0c06746⟩
International audience; In organometallic chemistry, and especially in the catalysis area, accessing the finest tuning of a catalytic reaction pathway requires a detailed knowledge of the steric and electronic influence of the ligands bound to the me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cfe17fe946fac32d00fcb3bc2888e92
https://hal.archives-ouvertes.fr/hal-02997117
https://hal.archives-ouvertes.fr/hal-02997117
Publikováno v:
New Journal of Chemistry
New Journal of Chemistry, Royal Society of Chemistry, 2020, 44, pp.14373-14378. ⟨10.1039/D0NJ02923H⟩
New Journal of Chemistry, 2020, 44, pp.14373-14378. ⟨10.1039/D0NJ02923H⟩
New Journal of Chemistry, Royal Society of Chemistry, 2020, 44, pp.14373-14378. ⟨10.1039/D0NJ02923H⟩
New Journal of Chemistry, 2020, 44, pp.14373-14378. ⟨10.1039/D0NJ02923H⟩
2-Substituted 1,3-indandione derivatives are known to undergo a photochemical rearrangement into phthalides. We find that in the presence of a substituent involving a double carbon–carbon bond in the vicinity of the carbonyl group in spiro-1,3-inda
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52af4f07d84b3786738e94e2ac7fb49a
https://hal.archives-ouvertes.fr/hal-02909637/file/HAL.pdf
https://hal.archives-ouvertes.fr/hal-02909637/file/HAL.pdf