2009年
■ Modular synthesis of the ClickFerrophos ligand family and their use in rhodium- and ruthenium-catalyzed asymmetric hydrogenetion
Oki, Hiroshi; Oura, Ichiro; Nakamura, Tatsuhito; Ogata, Kenichi; Shin-ichi, Fukuzawa.
Tetrahedron Asymmetry (2009), 20, 2185-2191
■ Synthesis of Novel Ferrocenyl-Based P,S Ligands (ThioClickFerrophos) and Their Use in Pd-Catalyzed Asymmetric Allylic Substitutions
Kato, Minoru; Nakamura, Tatsuhito; Ogata, Ken-ichi; Fukuzawa, Shin-ichi.
European Journal of Organic Chemistry (2009), (30), 5232-5238.
[Highlighted in Bibliographic Notebooks For Organometallic Chemistry as Cover Picture]
■ Highly Chemoselective Nickel-Catalyzed Three-Component Cross-Trimerization of Three Distinct Alkynes Leading to 1,3-Dien-5-ynes
Ogata, Kenichi; Sugasawa, Jun; Fukuzawa, Shin-ichi.
Angewandt Chemie International Edition (2009), 48, 6078-6080
■ Copper-ClickFerrophos-Complex-Catalyzed Enantioselective Reductive Aldol Reaction
Kato, Minoru; Oki, Hiroshi; Ogata, Ken-ichi; Fukuzawa, Shin-ichi.
Synlett (2009), 1299-1302
■ Copper-Catalyzed direct thiolation of benzoxazole with diaryl disulfides and aryl thiols
Fukuzawa, Shin-ichi; Shimizu, Eiji; Atsuumi, Yuka; Haga, Masatake; Ogata, Ken-ichi.
Tetrahedron Letters (2009), 50, 2374-2376
■ Nickel-Catalyzed Highly Regio- and Stereoselective Cross- Trimerization between Triisopropylsilylacetylene and Internal Alkynes Leading to 1,3-Diene-5-ynes
Kenichi, Ogata; Hiroyuki, Murayama; Jun, Sugasawa; Noriyuki, Suzuki; Shin-ichi, Fukuzawa.
Journal of the American Chemical Society (2009), 131(9), 3176-3177
[Highlighted in SYNFACTS]
■ Divalent Samarium Triflate Mediated Stereoselective Pinacol Coupling of Planar Chiral Phosphanyl and Phosphoryl Ferrocenecarbaldehyde
Fukuzawa, Shin-ichi; Oura, Ichiro; Shimizu, Kenta; Kato, Minoru; Ogata, Ken-ichi.
European Journal of Organic Chemistry (2009), (5), 716-720.
■ Copper(I)-Catalyzed Direct Arylation of 1,4-Disubstituted 1,2,3-Triazoles with Aryl Iodides
Fukuzawa, Shin-ichi; Shimizu, Eiji; Ogata, Kenichi.
Heterocycles (2009), 78 (3), 645-655.