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Department of Synthetic Chemistry, School of Engineering, Okayama University | 論文
- PB185 Synthesis of Some Natural Products via the Chiral Reduction of Ketones with Bakers' Yeast
- A highly stereoselective synthesis of (E)-enol lactones by the Wittig reaction of cyclic anhydrides with (.ALPHA.-alkoxycarbonyl-ethylidene)triphenylphosphorane.
- Solvolysis in carboxamides. II. Solvolytic elimination of 7.BETA.-methylbicyclo[3.3.1]non-3.BETA.-yl tosylate in carboxamides.
- A new method for the synthesis of 3,5-disubstituted 2(5H)-furanones. Synthesis of (.+-.)-acarenoic acid.
- Oxidation of 2,4-alkadienoic esters with selenium dioxide. A new synthesis of furans and selenophenes.
- Electrochemical reduction of exo-5-acetyl-endo-6-trichloromethylbicyclo[2.2.1]hept-2-ene.
- A new kinetic model for temperature programed thermogravimetry and its applications to the gasification of coal chars with steam and carbon dioxide.
- A new synthesis of 4-methoxy-6-valeryl-5,6-dihydro-2-pyrone.
- Diels-AIder Reactions of 5,5,5-Trichloro-3-penten-2-one and Related Compounds
- t-BuCl-NaI as a reagent for the selective reduction of olefinic double bond of .BETA.-phenyl .ALPHA.,.BETA.-unsaturated carbonyl compounds.
- A convenient synthesis of 4-(2,2-dichloroethenyl)-5,5-dimethyl-tetrahydro-2-furanone derivatives, a key intermediate of permethrinic acid.
- A Michael addition-induced Favorskii rearrangement.
- Synthesis of 5-[(E)-1-alkenyl]-3(2H)-furanones by the stereoselective dehydration with Me3SiCl.
- The Base-catalyzed Condensation of α-Haloaldehydes with Dichloroacetates
- Asymmetric reduction of .ALPHA.-(dimethylthiocarbamoylthio) carbonyl compounds with bakers' yeast.
- Highly enantioselective reduction of ethyl 2-acyloxy-3-oxobutanoate with immobilized Baker's yeast.
- Solvolysis of cis- and trans-4-t-Butylcyclohexyl Tosylates in N-Methylacetamide. Rates and Products Distribution
- Favorskii-type rearrangement of .ALPHA., .ALPHA.'-dihalo ketones induced by enolates of (diethoxyphosphinyl)acetic esters and its application to the synthesis of .ALPHA., .ALPHA.'-divinyl ketones.
- Favorskii-type rearrangement of .ALPHA.,.ALPHA.'-dihalo ketones with sodiomalonates leading to conjugated enone derivatives.
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