Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Marie-Laure Louillat"'
Autor:
Amira Sayed Khan, Aziz Hichami, Babar Murtaza, Marie-Laure Louillat-Habermeyer, Christophe Ramseyer, Maryam Azadi, Semen Yesylevskyy, Floriane Mangin, Frederic Lirussi, Julia Leemput, Jean-Francois Merlin, Antonin Schmitt, Muhtadi Suliman, Jérôme Bayardon, Saeed Semnanian, Sylvain Jugé, Naim Akhtar Khan
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 15, Iss 3, Pp 633-663 (2023)
Background & Aims: The spontaneous preference for dietary lipids is principally regulated by 2 lingual fat taste receptors, CD36 and GPR120. Obese animals and most of human subjects exhibit low orosensory perception of dietary fat because of malfunct
Externí odkaz:
https://doaj.org/article/faac987bf7904e528f779ff44b123109
Autor:
Maryam Rahimi, Bas de Bruin, Marie-Laure Louillat-Habermeyer, Harald Kelm, Monalisa Goswami, Frederic W. Patureau, Alexander Konkel, Rongwei Jin
Publikováno v:
Chemistry-A European Journal, 24(46), 11936-11943. Wiley-VCH Verlag
Chemistry-A European Journal
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry-A European Journal
Chemistry (Weinheim an Der Bergstrasse, Germany)
The straightforward capture of oxidized phenothiazines with phenols under aerobic conditions represents a unique cross‐dehydrogenative C−N bond‐forming reaction in terms of operational simplicity. The mechanism of this cross‐dehydrogenative N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::872c9db92ca2910c097ede7ebd47b950
https://doi.org/10.1002/chem.201800730
https://doi.org/10.1002/chem.201800730
Autor:
Frederic W. Patureau, Harald Kelm, Rongwei Jin, Alexander Konkel, Marie-Laure Louillat-Habermeyer, Bas de Bruin, Maryam Rahimi, Monalisa Goswami
Publikováno v:
Chemistry – A European Journal. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85f5562b5be3c03c698b5c699c5ae52d
https://doi.org/10.1002/chem.201884669
https://doi.org/10.1002/chem.201884669
Publikováno v:
Advanced Synthesis & Catalysis. 357:945-949
An unprecedented direct dehydrogenative ring closure of N-arylcarbazoles is achieved using a super-oxidative palladium-catalyzed C—H activation method.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b105ba6278ea5d0938fa70595063db40
https://doi.org/10.1002/adsc.201401136
https://doi.org/10.1002/adsc.201401136
Autor:
Marie-Laure Louillat-Habermeyer, Christophe Heitz, Bünyamin S. Oezkaya, Christina L. Bub, Alexander W. Jones, Frederic W. Patureau, Victoria Wagner
Publikováno v:
Chemistry - A European Journal. 22:17980-17982
The Ru catalyzed cross-dehydrogenative C-O bond formation between anilines and phenols is described and discussed. The exclusive C-O versus C-N bond-formation selectivity, moreover in the absence of chelating-assisting directing groups and while leav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73301322c18865826b09fd24f6a9c9e2
https://doi.org/10.1002/chem.201604764
https://doi.org/10.1002/chem.201604764
Publikováno v:
Organic Letters. 15:164-167
The cooperative action of Ru and Cu catalysts enables direct polynuclear C-H and N-H activation for the dehydrogenative N-carbazolation of carbazoles, selectively at the C1 position. Initial mechanistic experiments are presented and discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f9ab315327a7dcf3988cb755f57f580
https://doi.org/10.1021/ol303216u
https://doi.org/10.1021/ol303216u
Publikováno v:
ChemInform. 46
The direct dehydrogenative construction of C—N bonds between unprotected phenols and a series of cyclic anilines is achieved without any kind of metal activation of either substrate and without use of halides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a46002730ee25a776c6ccab99aee474
https://doi.org/10.1002/chin.201530100
https://doi.org/10.1002/chin.201530100
Publikováno v:
ChemInform. 46
An unprecedented direct dehydrogenative ring closure of N-arylcarbazoles is achieved using a super-oxidative palladium-catalyzed C—H activation method.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d797d8f3eb422aa346f73873caf8aba
https://doi.org/10.1002/chin.201530173
https://doi.org/10.1002/chin.201530173
Publikováno v:
Angewandte Chemie (International ed. in English). 54(13)
A method was developed for the direct dehydrogenative construction of CN bonds between unprotected phenols and a series of cyclic anilines without resorting to any kind of metal activation of either substrate and without the use of halides. The re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e617d65ff61439cd66556a57c662d969
https://pubmed.ncbi.nlm.nih.gov/25655504
https://pubmed.ncbi.nlm.nih.gov/25655504
Publikováno v:
ChemInform. 45
Towards “Oxidative-Ullmann–Goldberg” and “Oxidative-Buchwald–Hartwig” type amination reactions. This review focuses on the newly developed oxidative C–N bond formation techniques, applicable in the field of organic synthesis. Particular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9b6feb12542a28c61c2f4647ec72510
https://doi.org/10.1002/chin.201417273
https://doi.org/10.1002/chin.201417273