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81Yasufumi WadaJSPS Research Fellow., Kouji Otani, Noriko Endo, Yasuyuki KitaPresent address: Faculty of Pharmaceutical Sciences, Ritsumeikan University, 1-1-1 Nojihigashi, Kusatsu, Shiga, 525-8577. and Hiromichi Fujioka.
Novel dienone-phenol type rearrangement of 4,4-disubstituted cyclohexadienone system using thiosilane, Chem. Commun., 2010, 46, 797. Hiromichi Fujioka, Hideyuki Komatsu, Taeko Nakamura, Akihito Miyoshi, Kayoko Hata, Jnashuara Ganesh, Kenichi Murai and Yasuyuki Kita.
Organic synthesis using a hypervalent iodine reagent: unexpected and novel domino reaction leading to spiro cyclohexadienone lactones, Chem. Commun., 2010, 46, 4133. Arun Kumar Sundaresan, Lakshmi S. Kaanumalle, Corinne L. D. Gibb, Bruce C. Gibb and V. Ramamurthy.
Chiral photochemistry within a confined space: diastereoselective photorearrangements of a tropolone and a cyclohexadienone included in a synthetic cavitand, Dalton Trans., 2009, 4003. Rodolfo Tello-Aburto, Kyle A. Kalstabakken, Kelly A. Volp and Andrew M. Harned.
Regioselective and stereoselective cyclizations of cyclohexadienones tethered to active methylene groups, Org. Biomol. Chem., 2011, 9, 7849. Ghislain Deslongchamps and Pierre Deslongchamps.
Bent bonds, the antiperiplanar hypothesis and the theory of resonance. A simple model to understand reactivity in organic chemistry, Org. Biomol. Chem., 2011, 9, 5321. Toshifumi Dohi, Tomofumi Nakae, Yohei Ishikado, Daishi Kato and Yasuyuki Kita.
New synthesis of spirocycles by utilizing in situ forming hypervalent iodine species, Org. Biomol. Chem., 2011, 9, 6899. Electrochemical reduction of 4-methyl-4-(trichloromethyl)cyclohexa-2,5-dien-1-one, Russian Journal of General Chemistry Spin state of cyclohexadienone caebenes, Bulletin of the Academy of Sciences of the USSR, Division of chemical science Reaction of 4-chlorohexafluoro-2,5-cyclohexadienyl fluorosulfate and hexafluoro-2,5-cyclohexadienylene 1,4-bis(fluorosulfate) with nucleophilic reagents, Bulletin of the Academy of Sciences of the USSR, Division of chemical science Sterically hindered phenols, Bulletin of the Academy of Sciences of the USSR, Division of chemical science