0000000001158960
AUTHOR
Johan Guilbaud
showing 5 related works from this author
Palladium-catalyzed heteroaryl thioethers synthesis overcoming palladium dithiolate resting states inertness: Practical road to sulfones and NH-sulfo…
2018
International audience; We provide efficient synthetic access to heteroaryl sulfones in two-steps using a simple palladium-1,1'-bis [(diphenyl)phosphanyl]ferrocene catalyst to form in high yields variously functionalized heteroaromatic thioethers. Pyridinyl-containing substrates can be subsequently selectively oxidized into sulfones and NH-sulfoximines by using very mild oxidation conditions with a high functional group tolerance. In the palladium catalyzed C-S coupling of heteroaromatic thiols, reactivity limitation is attached with electron-deficient thiols. We show that this limitation can be resolved by the successful use of 2-bromoheteroarenes in the C-S coupling. We established herein…
(2-Pyridyl)sulfonyl Groups for ortho -Directing Palladium- Catalyzed Carbon-Halogen Bond Formation at Functionalized Arenes
2017
International audience; We describe an efficient palladium-catalyzed selective C-H ortho-monohalogenation (X=I, Br, Cl, F) of various functionalized (2-pyridyl) aryl-sulfones. ortho-, meta-and para-functionalization is tolerated at the arene group which undergoes C-H halogenation. Some modifications are also possible on the 2-(arylsulfonyl) heteroaryl directing groups. A comparison of the halogenation efficiency suggests that bromination is the practical method of choice, while chlorination and fluorination are possible but more challenging. Under forcing conditions ortho-dihalogenation can also be achieved.
C–H Halogenation of Pyridyl Sulfides Avoiding the Sulfur Oxidation: A Direct Catalytic Access to Sulfanyl Polyhalides and Polyaromatics
2019
Palladium-catalyzed oxidative C–H halogenation and acetoxylation reactions of S-unprotected sulfides, selectively directed by pyridinyl groups, allows the formation of C–X bonds (X = I, Br, Cl, OAc) by using simple halosuccinimide or phenyliodine diacetate (PIDA) oxidants. The undesired formation of sulfoxides and/or sulfones, which are usually observed under oxidative conditions, is fully obviated. Under the solvent-dependent conditions that we proposed, sulfide C–H functionalization is achieved in less than 1 h without any direct electrophilic halogenation at the pyridine moiety. N-Directed ortho-C–H activation of aryl also facilitates dibromination reactions which are hardly accessible w…
Halogenated (arylsulfanyl)pyridines syntheses and their derivatives by C-S and C-X couplings catalyzed by palladium complexes
2018
C–H activation of aryl compounds directed by 2-sulfonylpyridine and 2-sulfanylpyridine moiety for the formation of C–X (X = F, Cl, Br, I) bonds was studied. First, the syntheses of thioethers (2-(arylsulfanyl)pyridines) and sulfones (2-(arylsulfonyl)pyridines) were necessary for the progress of this project. A C–S coupling catalyzed by palladium complexe between thioaryls and halogenated heterocycles was performed for the synthesis of thioethers. The cheap ligand bis(diphenylphosphino)ferrocene (dppf) was used for this convenient reaction. Then, oxidation of thioethers was performed to synthesize sulfones. Halogenation of these compounds was studied with ortho-directed C–H activation cataly…
CCDC 1558706: Experimental Crystal Structure Determination
2017
Related Article: Johan Guilbaud, Marine Labonde, Hélène Cattey, Sylvie Contal, Christian Montalbetti, Nadine Pirio, Julien Roger, Jean-Cyrille Hierso|2017|Adv.Synth.Catal.|359|3792|doi:10.1002/adsc.201700858