TEMPO-Mediated Oxidation of Primary Alcohols to Carboxylic Acids by Exploitation of Ethers in an Aqueous-Organic Biphase System
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概要
- 論文の詳細を見る
- Chemical Society of Japanの論文
- 2009-08-15
著者
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Mei Zhen-wu
Department Of Medical And Bioengineering Science Graduate School Of Natural Science And Technology O
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Ma Li-jian
Department Of Medical And Bioengineering Science Graduate School Of Natural Science And Technology O
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KAWAFUCHI Hiroyuki
Department of Chemical and Biochemical Engineering, Toyama National College of Technology
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OKIHARA Takumi
Department of Material Chemistry, Graduate School of Natural Science and Technology, Okayama Univers
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INOKUCHI Tsutomu
Department of Medical and Bioengineering Science, Graduate School of Natural Science and Technology,
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Inokuchi Tsutomu
Department Of Medical And Bioengineering Science Graduate School Of Natural Science And Technology O
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Inokuchi Tsutomu
Department Of Applied Chemistry Faculty Of Engineering Okayama University
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Okihara Takumi
Department Of Material Chemistry Graduate School Of Natural Science And Technology Okayama Universit
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Kawafuchi Hiroyuki
Department Of Chemical And Biochemical Engineerings Toyama National College Of Technology
関連論文
- TEMPO-Mediated Oxidation of Primary Alcohols to Carboxylic Acids by Exploitation of Ethers in an Aqueous-Organic Biphase System
- Synthesis of dl-Shikonin by Vanadium(II)-Assisted Cross-Coupling and Electrooxidation of Aromatic Nuclei
- Oxidations of Dihydroxyalkanoates to Vicinal Tricarbonyl Compounds with a 4-BzoTENPO-Sodium Bromite System or by Indirect Electrolysis Using 4-BzoTEMPO and Bromide Ion
- Diastereoselective Michael Addition of Magnesium Amide to O-(2-Alkenoyl)TEMPOs and Comparison of Reactivity with Acyl Substituent-Modified Carboxylic Analogues
- Removal of α-Hydroxy Group of Acyloins and Their Derivatives with Vanadium(II) - THF Complex
- Electrochemical Wacker Type Reaction with a Double Mediatory System Consisting of Palladium Complex and Tri(4-bromophenyl)amine
- Electrogenerated acid-catalyzed Michael reaction of enol silyl ethers and ketene silyl acetals to .ALPHA.,.BETA.-unsaturated carbonyl compounds.
- Electrogenerated acid-assisted preparation of ethers from aldehydes and ketones.
- Electrogenerated acid-catalyzed reactions of acetals, aldehydes, and ketones with organosilicon compounds, leading to aldol reactions, allylations, cyanations, and hydride additions.
- A straightforward access to 5-deoxy-D-arabinono-1,4-lactone, a versatile intermediate in the lauraceae lactones syntheses.
- Electrogenerated acid as an efficient catalyst for the protection and deprotection of alcohols with dihydropyran and transesterification of glyceride.
- A new oxidizing system for aromatic alcohols by the combination of N-oxoammonium salt and electrosynthesized tetraalkylammonium tribromide.
- Indirect electrooxidation of halohydrins by a double mediatory system of Ru(VIII)/Ru(IV) and (Cl+)/Cl-. Optimization for the oxidation of 1,3-dichloro-2-propanol to 1,3-dichloroacetone.
- Functionalization of trans-decalin. IV. A stereoselective synthesis of dl-.BETA.-costol, dl-arctiol, and the related eudesmane type sesquiterpenes.
- Synthesis of lepiochlorin, a chlorinated antibiotic, by use of electrochemical haloalkoxylation.
- The cross-aldol reaction of 3-alkoxy-2-cyclohexen-1-ones with .ALPHA.,.BETA.-enals. A synthesis of 4-(trans-2-butenylidene)-3,5,5-trimethyl-2-cyclohexen-1-ones.
- Functionalization of trans-decalin. II. A synthesis of dl-isopetasol from trans-5-oxodecalin-8a,2-carbolactone.
- Indicrect electrooxidation by using ruthenium tetraoxide and chloride ion as recycling mediators. Optimization for the oxidation of diisopropylidene-D-glucose to the ulose.