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Kuroboshi, Manabu, Ishihara, Takashi (1990) An Efficient and General Method for the Reformatsky-Type Reaction of Chlorodifluoromethyl Ketones with Carbonyl Compounds Giving α,α-Difluoro-β-hydroxy Ketones. Bulletin of the Chemical Society of Japan, 63 (2). 428-437 doi:10.1246/bcsj.63.428

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Reference TypeJournal (article/letter/editorial)
TitleAn Efficient and General Method for the Reformatsky-Type Reaction of Chlorodifluoromethyl Ketones with Carbonyl Compounds Giving α,α-Difluoro-β-hydroxy Ketones
JournalBulletin of the Chemical Society of Japan
AuthorsKuroboshi, ManabuAuthor
Ishihara, TakashiAuthor
Year1990 (February)Volume63
Issue2
PublisherThe Chemical Society of Japan
DOIdoi:10.1246/bcsj.63.428Search in ResearchGate
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Mindat Ref. ID4496578Long-form Identifiermindat:1:5:4496578:7
GUID0
Full ReferenceKuroboshi, Manabu, Ishihara, Takashi (1990) An Efficient and General Method for the Reformatsky-Type Reaction of Chlorodifluoromethyl Ketones with Carbonyl Compounds Giving α,α-Difluoro-β-hydroxy Ketones. Bulletin of the Chemical Society of Japan, 63 (2). 428-437 doi:10.1246/bcsj.63.428
Plain TextKuroboshi, Manabu, Ishihara, Takashi (1990) An Efficient and General Method for the Reformatsky-Type Reaction of Chlorodifluoromethyl Ketones with Carbonyl Compounds Giving α,α-Difluoro-β-hydroxy Ketones. Bulletin of the Chemical Society of Japan, 63 (2). 428-437 doi:10.1246/bcsj.63.428
In(1990, February) Bulletin of the Chemical Society of Japan Vol. 63 (2) The Chemical Society of Japan

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Kuroboshi, Manabu, Ishihara, Takashi (1990) Diastereoselective Reduction of α,α-Difluoro β-Hydroxy Ketones tosyn- andanti-2,2-Difluoro-1,3-diols. Bulletin of the Chemical Society of Japan, 63 (4). 1185-1190 doi:10.1246/bcsj.63.1185
Ishihara, Takashi, Yamanaka, Tohru, Ando, Teiichi (1984) NEW LOW-VALENT TITANIUM CATALYZED REACTION OF CHLORODIFLUOROMETHYL KETONES LEADING TO α,α-DIFLUORINATED β-HYDROXY KETONES. Chemistry Letters, 13 (7). 1165-1168 doi:10.1246/cl.1984.1165
Kuroboshi, Manabu, Ishihara, Takashi (1990) An Efficient Generation and Selective Aldol Reaction of the Boryl Enolates ofN,N-Dialkyl-2,3,3,3-tetrafluoropropanamides. Bulletin of the Chemical Society of Japan, 63 (4). 1191-1195 doi:10.1246/bcsj.63.1191
Nitta, Makoto, Soeda, Hironobu, Iino, Yukio (1990) On the Reaction ofN-[(3-Oxo-2-cyclohexenyl)imino]triphenylphosphorane with α-Bromo Ketones and α,β-Unsaturated Ketones. Bulletin of the Chemical Society of Japan, 63 (3). 932-934 doi:10.1246/bcsj.63.932
Ishihara, Takashi, Kuroboshi, Manabu (1987) Zinc(0)–Copper(I) Chloride Promoted Reaction of Methyl Dichlorofluoroacetate with Carbonyl Compounds. A New Efficient Method for the Synthesis of Methyl (Z)-α-Fluoro-α,β-unsaturated Carboxylates. Chemistry Letters, 16 (6). 1145-1148 doi:10.1246/cl.1987.1145
Tsuji, Tadakazu (1989) Acid-Catalyzed Oxidation of Oxiranes with Dimethyl Sulfoxide Giving α-Hydroxy Ketones. Bulletin of the Chemical Society of Japan, 62 (2). 645-647 doi:10.1246/bcsj.62.645
Inokawa, Hiromi (1964) The Reaction Mechanism of α-Bromo-α, β-unsaturated Ketones with Amines. Bulletin of the Chemical Society of Japan, 37 (4). 568-570 doi:10.1246/bcsj.37.568
ISHIHARA, T., YAMANAKA, T., ANDO, T. (1985) ChemInform Abstract: NEW LOW-VALENT TITANIUM CATALYZED REACTION OF CHLORODIFLUOROMETHYL KETONES LEADING TO α,α-DIFLUORINATED β-HYDROXY KETONES. Chemischer Informationsdienst, 16 (3) doi:10.1002/chin.198503154
Yokoyama, Tai, Nohara, Fujio (1965) The Peracid Oxidation of Ketones. III. The Reaction of α,β-Unsaturated Ketones with Peroxybenzoic Acid. Bulletin of the Chemical Society of Japan, 38 (9). 1498-1500 doi:10.1246/bcsj.38.1498
Sato, Kikumasa, Kurihara, Yoshie, Inoue, Seiichi (1967) Reaction of Aliphatic Ketones with α-Cyano-α, β-unsaturated Acid Derivatives. Bulletin of the Chemical Society of Japan, 40 (4). 942-945 doi:10.1246/bcsj.40.942
Sugita, Toshio, Gohda, Katsura, Kagiya, Tsutomu (1990) Thermodynamic Stability of β-Chloro-, β-Phenylthio-, and β-Phenylamino-Substituted α,β and β,γ-Unsaturated Ketones. Bulletin of the Chemical Society of Japan, 63 (1). 278-280 doi:10.1246/bcsj.63.278
 
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