PULBLICATIONS
Ruthenium-Catalysed Cross-Coupling Reaction of Ketones with Transformable Directing Groups as Alkenyl Electrophiles
Yuya Kogure, Kohei Hatakeyama, Kai Tsuchiya, Yuta Kunii, and Satoshi Ueno,*
Chem. Commun., Advance Article (Sep. 25, 2023).
Synthesis of β-Enaminones via Palladium-Catalyzed Dehydrogeantive β-Amination of Saturated Ketones
Satoshi Ueno,* Shohei Yasuoka, Ryo Minamikawa, and Ryoichi Kuwano,*
Chem. Lett., Web Released (Sep. 1, 2023).
Palladium-Catalyzed para-Selective Allylation of 1-(Cyanomethyl)arenes with Allyl Acetates
Rina Muto, Kenji Nagata, Yoshiki Nakazumi, Kaho Nakamura, and Satoshi Ueno,*
Org. Lett., 25 (12), 2108–2112 (2023).
One-Pot Synthesis of Substituted Pyridines from Alkyl Ketones and Enamines by the Nickel-Catalyzed Dehydrogenation of Alkyl Ketones
Satoshi Ueno,* Ryohei Maeda, Yuya Kogure, and Ryoichi Kuwano,*
Chem. Lett., 52 (3), 148–151 (2023).
DOI: 10.1246/cl.220546 (Open Access)
(Selected as one of the Daily Top Accessed Articles in Chem. Lett., Mar. 2023)
Ruthenium-Catalyzed Cross-Coupling of Ketones as an Alkenyl Electrophile with Organoborons via Cleavage of Alkenyl C–N Bonds of in Situ Generated Enamines
Yuya Kogure and Satoshi Ueno,*
Org. Lett., 24 (50), 9233–9237 (2022).
DOI: 10.1021/acs.orglett.2c03765
(Selected as one of the Monthly Top 20 Most Read Articles in Org. Lett., Jan. 2023)
Diamine-Promoted Deacylation of 2-Alkyl-1,3-Diketones for the Facile Synthesis of Ketones
Rei Ishihara, Kota Okamura, Yuki Yoshimura, and Satoshi Ueno,*
ChemistrySelect, 7 (37), e202202717 (2022).
One-Pot Synthesis of Multiarylated Benzophenones via [3 + 2 + 1] Benzannulation of Ketones, Alkynes, and α,β-Unsaturated Carbonyls
Shoko Nagahata, Seiya Takei, and Satoshi Ueno,*
J. Org. Chem., 87 (15), 10377–10384 (2022).
Palladium-Catalyzed Dehydrogenative [3+3] Aromatization of Propyl Ketones and Allyl Carbonates
Kenta Koike and Satoshi Ueno,*
Chem. Lett., 51 (4), 489–492 (2022).
DOI:10.1246/cl.220032 (Open Access)
(Selected as one of the Daily Top Accessed Articles in Chem. Lett., Apr. 2022)
Palladium-catalyzed Benzylic Substitution of Benzyl Carbonates with Phosphorus Nucleophiles
Yusuke Makida, Kazumi Usui, Satoshi Ueno, and Ryoichi Kuwano,*
Chem. Lett., 46 (12), 1814–1817 (2017).
β-Amination of Saturated Nitriles through Palladium-Catalyzed Dehydrogenation/1,4-Addition/Re-dehydrogenation
Satoshi Ueno,* Ryohei Maeda, Shohei Yasuoka, and Ryoichi Kuwano,*
Chem. Lett., 42 (1), 40–42 (2013).
Synthesis of 4-Quinolones through Nickel-Catalyzed Intramolecular Amination on the β-Carbon of o-(N-Alkylamino)propiophenones
Satoshi Ueno,* Ryosuke Shimizu, Ryohei Maeda, Ryoichi Kuwano,*
Synlett, 23 (11), 1639–1642 (2012).
Intramolecular SN’-Type Aromatic Substitution of Benzylic Carbonates at their Para-Position
Satoshi Ueno, Sadakazu Komiya, Takeshi Tanaka, and Ryoichi Kuwano,*
Org. Lett., 14 (1), 338–341 (2012).
Transformation of α-Substituted Propanols to γ-Amino Alcohols through Nickel-Catalyzed Amination on the Terminal γ-Carbon of Propanols
Satoshi Ueno,* Kazumi Usui, and Ryoichi Kuwano,*
Synlett, 2011 (9), 1303–1307 (2011).
Palladium-Catalyzed [4+2] Cycloaddition of o-(Silylmethyl)benzyl Esters with Ketones: An Equivalent to Oxo-Diels–Alder Reaction of o-Xylylenes
Satoshi Ueno, Masakazu Ohtsubo, and Ryoichi Kuwano,*
Org. Lett., 12 (19), 4332–4334 (2010).
Nickel-Catalyzed Formation of a Carbon–Nitrogen Bond at the β-Position of Saturated Ketones
Satoshi Ueno,* Ryosuke Shimizu, and Ryoichi Kuwano,*
Angew. Chem. Int. Ed., 48 (25), 4543–4545 (2009).
(Highlighted in SYNFACT and in Speciality Chemicals Magazine: February 2010 Chemistry Corner)
[4+2] Cycloaddition of o-Xylylenes with Imines Using Palladium Catalyst
Satoshi Ueno, Masakazu Ohtsubo, and Ryoichi Kuwano,*
J. Am. Chem. Soc., 131 (36), 12904–12905 (2009).
Direct, Iridium-Catalyzed Enantioselective and Regioselective Allylic Etherification with Aliphatic Alcohols
Satoshi Ueno and John F. Hartwig,*
Angew. Chem. Int. Ed., 47 (10), 1928–1931 (2008).
Enantioselective Iridium-Catalyzed Allylic Amination of Ammonia and Convenient Ammonia Surrogates
Mark J. Pouy, Andreas Leitner, Daniel J. Weix, Satoshi Ueno, and John F. Hartwig,*
Org. Lett., 9 (20), 3949–3952 (2007).
Unique Effect of Coordination of an Alkene Moiety in Products on Ruthenium-Catalyzed Chemoselective C–H Alkenylation
Satoshi Ueno, Takuya Kochi, Naoto Chatani, and Fumitoshi Kakiuchi,*
Org. Lett., 11 (4), 855–858 (2009).
Ruthenium-Catalyzed Carbon–Carbon Bond Formation via the Cleavage of an Unreactive Aryl Carbon–Nitrogen Bond in Aniline Derivatives with Organoboronates
Satoshi Ueno, Naoto Chatani, and Fumitoshi Kakiuchi,*
J. Am. Chem. Soc., 129 (19), 6098–6099 (2007).
Regioselective Alkenylation of Aromatic Ketones with Alkenylboronates Using a RuH2(CO)(PPh3)3-Catalyst via Carbon–Hydrogen Bond Cleavage
Satoshi Ueno, Naoto Chatani, and Fumitoshi Kakiuchi,*
J. Org. Chem., 72 (9), 3600–3602 (2007).
Direct Observation of the Oxidative Addition of the Aryl Carbon–Oxygen Bond to a Ruthenium Complex and Consideration of the Relative Reactivity between Aryl Carbon–Oxygen and Aryl Carbon–Hydrogen Bonds
Satoshi Ueno, Eiichiro Mizushima, Naoto Chatani, and Fumitoshi Kakiuchi,*
J. Am. Chem. Soc., 128 (51), 16516–16517 (2006).
Ruthenium-Catalyzed Functionalization of Aryl Carbon–Oxygen Bonds in Aromatic Ethers with Organoboron Compounds
Fumitoshi Kakiuchi,* Mayumi Usui, Satoshi Ueno, Naoto Chatani, and Shinji Murai,
J. Am. Chem. Soc., 126 (9), 2706–2707 (2004).