H
Henri Doucet
Researcher at University of Rennes
Publications - 471
Citations - 11517
Henri Doucet is an academic researcher from University of Rennes. The author has contributed to research in topics: Catalysis & Aryl. The author has an hindex of 53, co-authored 461 publications receiving 10715 citations. Previous affiliations of Henri Doucet include University of Oxford & Jinan University.
Papers
More filters
Journal ArticleDOI
Palladium-based catalytic systems for the synthesis of conjugated enynes by Sonogashira reactions and related alkynylations
Henri Doucet,Jean-Cyrille Hierso +1 more
TL;DR: This Review gives an overview of the highly efficient palladium catalyst systems for the direct alkynylation of C(sp(2)) halides with terminal alkynes, both in homogeneous and heterogeneous phases.
Journal ArticleDOI
trans‐[RuCl2(phosphane)2(1,2‐diamine)] and Chiral trans‐[RuCl2(diphosphane)(1,2‐diamine)]: Shelf‐Stable Precatalysts for the Rapid, Productive, and Stereoselective Hydrogenation of Ketones
Henri Doucet,Takeshi Ohkuma,Kunihiko Murata,Tohru Yokozawa,Masami Kozawa,Eiji Katayama,Anthony F. England,Takao Ikariya,Ryoji Noyori +8 more
TL;DR: Carbononyl-selective asymmetric hydrogenation of α,β-unsaturated ketones proceeds in the presence of these RuII catalysts, and 4-substituted cyclohexanones are selectively converted into cis alcohols.
Journal ArticleDOI
Asymmetric Hydrogenation of Alkenyl, Cyclopropyl, and Aryl Ketones. RuCl2(xylbinap)(1,2-diamine) as a Precatalyst Exhibiting a Wide Scope
Takeshi Ohkuma,Masatoshi Koizumi,Henri Doucet,Trang Pham,Masami Kozawa,Kunihiko Murata,Eiji Katayama,Tohru Yokozawa,Takao Ikariya,Ryoji Noyori +9 more
Journal ArticleDOI
Palladium‐Catalyzed C3 or C4 Direct Arylation of Heteroaromatic Compounds with Aryl Halides by C ? H Bond Activation
TL;DR: Arylation at C 3 and C 4 positions of a C-H bond activation has become a popular method for generating carbon-carbon bonds as mentioned in this paper, and a wide variety of hetero-aromatics, such as furans, thiophenes, pyrroles, thiosoles, thiazoles, oxazoles, imidazoles and pyrazoles can be employed.
Journal ArticleDOI
Suzuki–Miyaura Cross-Coupling Reactions of Alkylboronic Acid Derivatives or Alkyltrifluoroborates with Aryl, Alkenyl or Alkyl Halides and Triflates
TL;DR: In this paper, the Suzuki-Miyaura cross-couplings of organoboronic acids or organotrifluoroborates with aryl and alkenyl halides or triflates have become classic methods for generating carbon-carbon bonds.