Hashimoto Harukichi | Department of Applied Chemistry, Faculty of Engineering, Tohoko University
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概要
- Hashimoto Harukichiの詳細を見る
- 同名の論文著者
- Department of Applied Chemistry, Faculty of Engineering, Tohoko Universityの論文著者
関連著者
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Hashimoto Harukichi
Department of Applied Chemistry, Faculty of Engineering, Tohoko University
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Miyano Sotaro
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Inoue Yoshio
Department Of Biomolecular Engineering Graduate School Of Engineering Tohoku University
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Miyano Sotaro
Department Of Biochemistry And Engineering Faculty Of Engineering Tohoku University
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Yamashita Junzo
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Handa Shigeru
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Hokari Hiroshi
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Handa Shigeru
Department Of Electronic Engineering Faculity Of Engineering Tohoku University
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Fukushima Hiroshi
Department Of Materials Science Faculty Of Engineering The University Of Tokyo:(present Address) Dep
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Mori Akira
Departmenet Of Animal Husbandry Faculty Of Agriculture Tohoku University
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Kondo Takashi
Department Of Agricultural Chemistry The University Of Tokyo
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Shimizu Kunitoshi
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Toyofuku Masanori
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Taguchi Masaaki
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Sato Michio
Department Of Electrical Communications Faculty Of Engineering Tohoku University
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Sato Shinya
Department Of Animal Science Tokyo University Of Agriculture
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ISHIKAWA Shinji
Department of Agricultural Chemistry, Faculty of Agriculture, Niigata University
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Ohno Yutaka
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Izumi Yu
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Fujii Katsuo
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Hashimoto Harukichi
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Tobita Masayuki
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Ito Hiromitsu
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Sato Shinya
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Tagami Katsuya
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Onuma Kazuhiko
Department of Synthetic Chemistry, The University of Tokyo
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Yamashita Junzo
Department of Synthetic Chemistry, The University of Tokyo
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Satake Masaki
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Nawa Masayoshi
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Ohtsuka Yukihiro
Department of Applied Chemistry, Faculty of Engineering, Tohoko University
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Itoh Yoshio
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Kazama Haruo
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Ohta Katsuaki
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Inagawa Hideho
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Umeda Yoshiharu
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
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Okada Shin-ichi
Department of Applied Chemistry, Faculty of Engineering, Tohoku University
著作論文
- The asymmetric Ullmann coupling reaction of chiral diol diesters of 1-bromo-2-naphthoic acid and 2-halo-3-nitrobenzoic acids: Highly diastereoselective synthesis of atropisomeric 6,6'-dinitrodiphenic acids.
- Carbon-carbon bond formation by use of chloroiodomethane as a C1 unit. I. Formation of chloromethyltriphenylphosphonium iodide, and its application for the Wittig chloromethylenation of aldehydes and ketones.
- Asymmetric synthesis of axially chiral, unsymmetrical diphenic acids via intramolecular Ullmann coupling reaction.
- The Ullmann coupling reaction of axially chiral (S)-2,2'-bis(1-iodo-2-naphthyloxycarbonyl)-1,1'-binaphthyl.
- Ultrasounds in synthetic reactions. II. Convenient methylenation of carbonyl compounds with zinc-diiodomethane.
- Base-catalyzed autoxidation of fluorene in the presence of phase transfer catalysts.
- The Reductive Coupling Reactions of Some Chloromethylbenzene Derivatives with Iron(II) and Copper(I) Complexes
- Ultrasounds in synthetic reactions. III. Reduction of organic halides with nickel(II) chloride-zinc-water.
- Palladium-catalyzed reaction of isoprene with water in presence of carbon dioxide and base.
- Axially dissymmetric bis(aminophosphine)s derived from 2,2'-diamino-1,1'-binaphthyl. Synthesis and application to rhodium(I)-catalyzed asymmetric hydrogenations.
- 2-Allylisourea as a starting material for palladium-catalyzed wittig-type allylidenation of aldehydes.
- The asymmetric Ullmann coupling reaction of (S)-2,2'-bis(1-bromo-2-naphthoyloxy)-1,1'-binaphthyl revisited. Formation of 24-membered optically pure cyclic dimer as well as 12-membered cyclic monomer.
- Reaction of dialkyl-substituted alkynes with carbon dioxide catalyzed by nickel(0) complexes. Incorporation of carbon dioxide in alkyne dimers and novel cyclotrimerization of the alkynes.
- Carbon-carbon bond formation by the use of chloroiodomethane as a C1 unit. IV. The Mannich reaction of ketones by means of dihalomethane and secondary amine.
- Carbon-carbon bond formation by the use of chloroiodomethane as a C1 unit. III. A convenient synthesis of the Mannich base from enol silyl ether by a combination of chloroiodomethane and N,N,N',N'-tetramethylmethanediamine.
- Direct N-allylation of amides with 2-allylisourea catalyzed by palladium(0).
- Selective oxidation of 2-bromo-m-xylene to 2-bromo-3-methylbenzoic acid or 2-bromoisophthalic acid.
- Reaction of allene with water catalyzed by palladium(0) in the presence of carbon dioxide.
- Carbon-carbon bond formation by the use of chloroiodomethane as a C1 unit. II. The preparation and synthetic application of 1-chloro-3-iodoheptane.
- 2-Allylisourea as an effective agent for direct .ALPHA.-allylation of ketone and aldehyde assisted by palladium(0) under neutral conditions.
- Oxygen-accelerated generation of the bromocarbenoid reagent of zinc from diethylzinc and bromoform. Bromocyclopropanes from olefins.