Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Axel Labattut"'
Autor:
Sandra Abi Fayssal, Timothée Naret, Julien Buendia, Axel Labattut, Vincent Huc, Cyril Martini, Emmanuelle Schulz
Publikováno v:
Advanced Synthesis & Catalysis. 364:947-957
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b2f8e60655f60e290855d915582aa87
https://doi.org/10.1002/adsc.202101204
https://doi.org/10.1002/adsc.202101204
Publikováno v:
Catalysts; Volume 12; Issue 10; Pages: 1098
Pd-catalysed reactions are amongst the most important in current chemistry. Consequently, very reactive catalysts were developed during the last decades, allowing very high conversions at low catalytic rates. However, decreasing Pd leaching in final
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19914dab07c58938ce24884c62e885f1
Autor:
Erika Adhel, Sandra Abi Fayssal, Vincent Huc, Axel Labattut, Cyril Martini, Emmanuelle Schulz, Diana Dragoe, Julien Buendia, Ibrahim Abdellah
Publikováno v:
Catalysts
Catalysts, MDPI, 2020, 10 (9), pp.1081. ⟨10.3390/catal10091081⟩
Volume 10
Issue 9
Catalysts, Vol 10, Iss 1081, p 1081 (2020)
Catalysts, MDPI, 2020, 10 (9), pp.1081. ⟨10.3390/catal10091081⟩
Volume 10
Issue 9
Catalysts, Vol 10, Iss 1081, p 1081 (2020)
We report here the synthesis and characterization of a new calix[8]arene-supported PEPPSI-IPr Pd polymetallic complex. This complex, showing greater steric hindrance around the Pd centers compared with previous calix[8]arene-based catalysts, demonstr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15edbd1cb41abad58ff0b1ec3f9c89bc
https://hal.archives-ouvertes.fr/hal-03052954/document
https://hal.archives-ouvertes.fr/hal-03052954/document
Autor:
Axel Labattut, Cyril Martini, Ibrahim Abdellah, Emmanuelle Schulz, Sandra Abi Fayssal, Vincent Huc, Julien Buendia
Publikováno v:
Reaction Chemistry & Engineering
Reaction Chemistry & Engineering, Royal Society of Chemistry, 2020, 5 (8), pp.1509-1514. ⟨10.1039/d0re00118j⟩
Reaction Chemistry & Engineering, Royal Society of Chemistry, 2020, 5 (8), pp.1509-1514. ⟨10.1039/d0re00118j⟩
International audience; Benzyloxycalix[8]arene is reported as a suitable macrocyclic support for Pd-NHC complexes, which catalyses CC crosscoupling reactions with high efficiency. Resulting PEPPSI-derived complexes, issued from a scalable synthetic p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f164723dfd41271ed1d11b418a636a90
https://hal.archives-ouvertes.fr/hal-03052943/document
https://hal.archives-ouvertes.fr/hal-03052943/document
Autor:
Pauline Kasongo, Axel Labattut, Emmanuelle Schulz, Cyril Martini, Régis Guillot, Vincent Huc, Ibrahim Abdellah
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 47(39)
Benzyloxycalix[8]arene supported catalysts bearing N-heterocyclic carbene palladium complexes on each subunit were readily synthesized. Intermediates and catalysts were fully characterized, allowing for a fine control of their structure. X-ray diffra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fef05dd6cd04704ba3eb65f4aadba0b8
https://pubmed.ncbi.nlm.nih.gov/30215659
https://pubmed.ncbi.nlm.nih.gov/30215659
Publikováno v:
The Journal of organic chemistry. 82(22)
The role of hypervalent iodine reagents as oxidants has been widely recognized for more than 20 years. As electrophilic species, they could also play the role of Lewis acids. While not surprising, this aspect of these reagents has not been fully cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf6ed53ddf3807cc76eeffda2b111aac
https://pubmed.ncbi.nlm.nih.gov/28770606
https://pubmed.ncbi.nlm.nih.gov/28770606