Sugiyama Shigeru | Institute of Advanced Material Study, 86, Kyushu University
スポンサーリンク
概要
関連著者
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Takeshita Hitoshi
Institute Of Advanced Material Study 86 Kyushu University
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Mori Akira
Institute For Materials Chemistry And Engineering Kyushu University
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Sugiyama Shigeru
Institute of Advanced Material Study, 86, Kyushu University
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Tian Guan
Institute of Advanced Material Study, 86, Kyushu University
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Mori Akira
Institute of Advanced Material Study, 86, Kyushu University
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Nakashima Hisataka
Graduate School of Engineering Sciences, 39, Kyushu University
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Mametsuka Hiroaki
Central Research Laboratories, Nippon Kokan Company, Ltd.
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Tomiyasu Kazushi
Institute of Advanced Material Study, 86, Kyushu University
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Kodama Mitsuaki
Pharmaceutical School of Tokushima Bunri University
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Kusaba Tomoyuki
Graduate School of Engineering Sciences, 39, Kyushu University
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Watanabe Hiroyasu
Graduate School of Engineering Sciences, 39, Kyushu University
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Yamaguchi Hiroyuki
College of Technology, Ibaraki University
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Higashi Miwako
College of Technology, Ibaraki University
著作論文
- Synthetic photochemistry. XLV. Photoconversion of 2-methylenehomobarrelenes to 9-methylenebarbaralanes.
- Synthetic photochemistry. XLVII. Formation and degenerate Cope rearrangement of 9-dicyanomethylenebarbaralane.
- The solid-phase 13C NMR spectra of several tropolone derivatives.
- The kinetic evidence of the concerted[1,9]sigmatropy for the acetyl migration in the 2-acetoxytropones. The NMR spectral analysis of the seven-fold degenerated acetotropy of hexaacetoxytropone.
- Superjacent and subjacent orbitals participations for kinetically-controlled cycloaddition reactions of 2H-cyclohepta[b]furan-2-ones and 8,8-dicyanoheptafulvene to 2,3-bis(methoxycarbonyl)-7-oxabicyclo[2.2.1]heptadiene.
- Novel preparation of 1- and 3-substituted bicyclo[3.2.2]nona-3,6,8-trien-2-ones from tropones and 2,3-bis(methoxycarbonyl)-7-oxabicyclo-[2.2.1]heptadiene by high-pressure cycloaddition-thermal cycloreversion procedure.
- Thermal cycloaddition reaction of tropone to 1,1-diethoxyethene. Structure revision of Cantrell's Diels-Alder adduct.