Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jean-Luc Débieux"'
Synthesis of Hexa-peri-hexobenzocoronenes Carrying Linear or Branched Perfluoroalkylated Side Chains
Publikováno v:
Synthesis. 2010:1123-1140
Substituted disc-shaped perfluoroalkylated hexa-peri-hexabenzocoronenes (HBC), known to self-assemble into conducting ordered architectures, were synthesized and characterized. A systematic variation of the linear or branched perfluoroalkylated side
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b8aed26abf23f16066c466acf40b735
https://doi.org/10.1055/s-0029-1218667
https://doi.org/10.1055/s-0029-1218667
Publikováno v:
European Journal of Organic Chemistry. 2007:2073-2077
We report here conditions which allow the photoacylation of primary, secondary and tertiary alcohols with N-acetyl-5,7-dinitroindoline under exceptionally mild conditions, at wavelengths harmless to most functional groups, including otherwise photose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84332921c3f7c4443f3ae294fd5b411f
https://doi.org/10.1002/ejoc.200600790
https://doi.org/10.1002/ejoc.200600790
Autor:
Philippe Larignon, Mario Serrano, Cecília Rego, Florence Fontaine, Eliane Abou-Mansour, Floriane L’Haridon, Montserrat Ramírez-Suero, Sibylle Farine, Christohpe Bertsch, Maryline Magnin-Robert, Julie Chong, Alessandro Spagnolo, Jean-Luc Débieux, M. Bénard-Gellon
Publikováno v:
Phytochemistry
Phytochemistry, 2015, 115, pp.207-215. ⟨10.1016/j.phytochem.2015.01.012⟩
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Phytochemistry, 2015, 115, pp.207-215. ⟨10.1016/j.phytochem.2015.01.012⟩
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Liquid chromatography-diode array screening of the organic extract of the cultures of 13 isolates of the fungus Neofusicoccum parvum, the main causal agent of botryosphaeria dieback of grapevine, showed similar metabolites. One strain was selected fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97c9f092d5e559bb474bfacdb199f44d
http://doc.rero.ch/record/257043/files/abm_pmn_sm3.pdf
http://doc.rero.ch/record/257043/files/abm_pmn_sm3.pdf
Autor:
Jean-Luc Débieux, Christian G. Bochet
An all-photochemical synthesis of OGP(10–14), the biologically active part of an osteogenic growth peptide, was performed. This required the preparation of photochemically activable amino acids containing a 5,7-dinitroindoline derivative on the C-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d80bf16030ec81a757e179857cc7095
http://doc.rero.ch/record/27948/files/boc_aps.pdf
http://doc.rero.ch/record/27948/files/boc_aps.pdf
Autor:
Christian G. Bochet, Jean-Luc Débieux
Publikováno v:
ChemInform. 41
The acylation reaction occupies a central role in biochemistry and organic synthesis. On the one hand, it is by this very reaction that amino acids successively assemble to form peptides and proteins, and on the other hand it is a major synthetic met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0ebbc2224223a0cdb04d3867c488345
https://doi.org/10.1002/chin.201035256
https://doi.org/10.1002/chin.201035256
Publikováno v:
ChemInform. 41
Substituted disc-shaped perfluoroalkylated hexa-perihexabenzocoronenes (HBC), known to self-assemble into conducting ordered architectures, were synthesized and characterized. A systematic variation of the linear or branched perfluoroalkylated side c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33a5549e3e9d79624afefcab23540770
https://doi.org/10.1002/chin.201022086
https://doi.org/10.1002/chin.201022086
Autor:
Christian G. Bochet, Jean-Luc Débieux
A range of N-protected-alpha-amino acyl-5,7-dinitroindolines 3a-z were prepared in good yields from commercially available N-protected-alpha-amino acids 1a-z by a two-step sequence of acylation and intramolecular amide N-arylation. Subsequent photoch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5a24d86a1bdd28defbd35c90b8b2d54
http://doc.rero.ch/record/13143/files/bochet_ppa.pdf
http://doc.rero.ch/record/13143/files/bochet_ppa.pdf
Ligands 1 and 2 underwent quantitative photooxidation when they were reacted with singlet oxygen sensitized by methylene blue. However, the quantitative reaction became self-sensitized for the compound Ru(1) wherein the ruthenium complex acted as a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e38f9671e8203274a5aa69f266e96e1
http://doc.rero.ch/record/8122/files/belser_qss.pdf
http://doc.rero.ch/record/8122/files/belser_qss.pdf
Publikováno v:
European Journal of Organic Chemistry. 2007:2027-2027
The cover picture shows the photochemically promoted acylation of alcohols under very mild conditions. The experimental protocol is extremely simple, thanks to the use of a benchtop photochemical reactor based on UV LEDs. The acyl transfer proceeds w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f006f9448735883477ae8e3720f1f791
https://doi.org/10.1002/ejoc.200790024
https://doi.org/10.1002/ejoc.200790024