Zobrazeno 1 - 10
of 199
pro vyhledávání: '"Olivier Baudoin"'
Autor:
Olivier Baudoin
Publikováno v:
CHIMIA, Vol 75, Iss 11, Pp 967-971 (2021)
In recent years, transition-metal-catalyzed C–H functionalization has emerged as a potentially greener alternative to classic cross-couplings and as a powerful tool to access complex functional molecules with improved step-economy. This short accou
Externí odkaz:
https://doaj.org/article/87e964336f1247f38c398c33d2bfd7b6
Publikováno v:
CHIMIA, Vol 75, Iss 1-2 (2021)
Externí odkaz:
https://doaj.org/article/c3955a08aec140d686bca0e1248a765b
Publikováno v:
CHIMIA, Vol 74, Iss 12 (2020)
Externí odkaz:
https://doaj.org/article/20e97f016a1a4813b04419a397bb688e
Publikováno v:
CHIMIA, Vol 74, Iss 3 (2020)
Externí odkaz:
https://doaj.org/article/c694c4332aa74908bf17e2f0b273b23f
Publikováno v:
CHIMIA, Vol 73, Iss 12 (2019)
Externí odkaz:
https://doaj.org/article/3fb7e7dc892443b7b8608398bf7cc092
Autor:
Olivier Baudoin
Publikováno v:
CHIMIA, Vol 70, Iss 11 (2016)
Site-selectivity remains a major challenge in metal-catalyzed C–H bond functionalization. Most existing strategies rely on the introduction of a directing group or on the intrinsic reactivity of the substrate. In this account article, we describe t
Externí odkaz:
https://doaj.org/article/fe86f0ce5c594db49103f7a969168480
The three-dimensional structure of carbohelicenes has fascinated generations of molecular chemists and has been exploited in a wide range of applications. Their strong circularly polarized luminescence has attracted considerable attention in recent y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db482d945515fe45d5b194dd1b44ccbe
https://edoc.unibas.ch/94917/
https://edoc.unibas.ch/94917/
Autor:
Ekaterina A. Martynova, Marco Zuccarello, Domenic Kronenberg, Marek Beliš, Agnieszka Czapik, Ziyun Zhang, Kristof Van Hecke, Marcin Kwit, Olivier Baudoin, Luigi Cavallo, Steven P. Nolan
Green and sustainable access to chiral and achiral gold-IBiox complexes is reported. The gold complexes were synthesized using a simple, air-tolerant, weak base protocol carried out in a green solvent. Their catalytic activity was examined in the hyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2af0c38746f838d8345a0c79d9f1d478
https://edoc.unibas.ch/95282/
https://edoc.unibas.ch/95282/
Autor:
Anton Kudashev, Olivier Baudoin
Publikováno v:
Chemistry – A European Journal. 27:17688-17694
A ligand-controlled site-selective C(sp; 3; )-H arylation of heteroaromatic ketones has been developed using Pd catalysis. The reaction occurred selectively at the α- or β-position of the ketone side-chain. The switch from α- to β-arylation was r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c4cfe0e3f4bc60355408ff93cb0897b
https://doi.org/10.1002/chem.202103467
https://doi.org/10.1002/chem.202103467
Publikováno v:
Angewandte Chemie (International Ed. in English)
Vicinal aminoalcohols are widespread structural motifs in bioactive molecules. We report the development of a new dioxazolone reagent containing a p‐nitrophenyldifluoromethyl group, which 1. displays a good safety profile; 2. shows a remarkably hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::321fb17528389cde44a01120213c380d
https://doi.org/10.1002/anie.202110019
https://doi.org/10.1002/anie.202110019