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Department of Synthetic Chemistry, Faculty of Engineering, Kyoto University | 論文
- PB64 INTRAMOLECULAR HYDROSILATION : A NEW STEREOCONTROLLED SYNTHETIC METHOD IN CARBOHYDRATE CHEMISTRY
- An Ab initio MO Study of the Fragmentation Mechanism of the Cycloglycylglycine Ion in Mass Spectrometry
- The Synthesis of 3,5,3'-Triisopropyl-D, L-thyronine
- Anionic Ring-Opening Polymerization of 1,2,2-Trimethyl-1-phenyl-1,2-disilacyclopentane
- Amino Silica Gels Acting as a Carbon Dioxide Absorbent
- 反応性原子団の展望と今後の問題
- Novel Naphthalene Derivatives Undergoing Thermal Valence Isomerization to hemi-Dewar-naphthalene
- PA159 ISOPRENYLCOUMARIN FROM MERRILLIA CALOXYLON
- Efficient electron flux conversion from strongly hydrophilic NADH model in the transmembrane electron transfer by flavolipid.
- Addition reaction of carboxylic anhydrides to the carbon-nitrogen double bond of unsubstituted cyclic imidates.
- Organofluorosilicates in organic synthesis. XVI. Synthesis of organo-pentafluorosilicates via the Diels-Alder, ene, and Friedel-Crafts reaction. Their transformations to organic halides and alcohols.
- Electron spin distributions and g-value shifts in the novel electron donors with 1,3-dithiole rings.
- Intramolecular orbital interactions in 6,6'-bi(1,4-dithiafulvenyl) studied by photoelectron spectroscopy.
- The Nickel-catalyzed Cyclodimerization of Butadiene. The Synthesis of 2-Methylenevinylcyclopentane and the Isomerization of 1,3,7-Octatriene
- Preparation and physicochemical properties of new linear .MU.-oxo bridged ruthenium(IV) and osmium(IV) porphyrin dimers.
- Thermochemical studies on 2,4,6-triisopropylbenzophenone and its photo-isomer, 3',5'-diisopropyl-4,4-dimethyl-3-phenyl-1,2-benzocyclobuten-3-ol. Evaluation of magnitude of light energy stored in the latter molecule.
- Formation of ketone diperoxides from ozonation of O-methyloximes.
- Facile synthesis of 2-phenyl-1,2-oxaphospholane and its related new compounds. The family of deoxophostones and deoxothiolphostones.
- Base-catalyzed Oxygenation of 2,6-Di-t-butylphenols. A Convenient Method for Preparation of p-Quinols
- Coumarin-4-carboxylic Acids from Coumaran-2,3-diones
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