O
Olivier Baudoin
Researcher at University of Basel
Publications - 152
Citations - 7096
Olivier Baudoin is an academic researcher from University of Basel. The author has contributed to research in topics: Catalysis & Palladium. The author has an hindex of 39, co-authored 147 publications receiving 6231 citations. Previous affiliations of Olivier Baudoin include University of California, San Diego & University of Lyon.
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Journal ArticleDOI
Totalsynthese von sanglifehrin a
Kyriacos C. Nicolaou,Jinyou Xu,Fiona Murphy,Sofia Barluenga,Olivier Baudoin,Heng-Xu Wei,David Gray,Takashi Ohshima +7 more
TL;DR: In this article, the Immunsuppressivum Sanglifehrin A wurde erstmals in einer Totalsynthese hergestellt, and der Aufbau der makrocyclischen Einheit der Zielverbindung gelang durch eine selektive intramolekulare Stille-Kupplung, and die Spirolactameinheit wurded durch Paterson-Aldolreaktion erhalten.
Journal ArticleDOI
A New Dioxazolone for the Synthesis of 1,2-Aminoalcohols via Iridium(III)-Catalyzed C(sp3)–H Amidation
TL;DR: In this paper, a new dioxazolone reagent containing a p-nitrophenyldifluoromethyl group was developed, which showed a remarkably high reactivity in the oxime-directed iridium(III)-catalyzed amidation of unactivated C(sp3)-H bonds.
Book ChapterDOI
Applications of Catalytic Organometallic C(sp3)–H Bond Functionalization
TL;DR: This review focuses on recent applications of C(sp3)–H bond functionalization strategies to the synthesis of biologically active and natural compounds.
Journal ArticleDOI
Synthesis of Conformationally Constrained Esters and Amines by Pd-Catalyzed α-Arylation of Hindered Substrates
TL;DR: In this paper, the α-arylation of sterically hindered silyl ketene acetals (SKAs) with aryl bromides occurs efficiently using Pd[P(t-Bu)3]2 as the optimal catalyst and ZnF2 as a promoter.
Journal ArticleDOI
Remote Construction of N‐Heterocycles via 1,4‐Palladium Shift‐Mediated Double C−H Activation
TL;DR: It is shown that o‐bromo‐N‐methylanilines undergo a 1,4‐Pd shift at the N‐methyl group, followed by intramolecular trapping and remote C−C bond formation to generate biologically relevant isoindolines and β‐lactams.