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Pharmaceutical Institute Medical Faculty University Of Tokyo | 論文
- WHY MOLECULAR FLUORINE ADDS TO ETHYLENES IN A CIS FASHION
- Latams. X. The Alkaline Ferricyanide Oxidation of 3-Substituted 1-(3,4-Dimethoxyphenethyl) pyridinium Salts : Effects of Functional Substituents
- Lactams. VIII. The Alkaline Ferricyanide Oxidation of 3-Substituted 1-(3,4-Dimethoxyphenethyl) pyridinium Salts : Effects of Hydrocarbon Substituents on Orientation of the Oxidation
- Lactams. VI. Synthesis and Nuclear Magnetic Resonance Study of 1-Aralkyl-3-methyl- and -5-methyl-2(1H)-pyridones
- 1-Methyl-3-ethylpyridinium塩の酸化(訂正)
- 3-置換1-Alkylpyridinium塩の酸化(第3報)1-Methyl-3-ethyl-6-pyridone及び-piperidoneの製法
- 3-置換1-Alkylpridinium塩の酸化(第2報)1-Methyl-及び1-Phenethyl-3-phenyl-pyridinium塩の酸化
- 鎮痙作用の薬品作用学的研究(第5報)ハツカネズミの摘出小腸によるアセチルコリン及びアトロピンの生物試験法の基礎的研究
- モルフィナン同族体の合成(第1報)3-Hydroxy-N-methyl-"C"-normorphinan及び-"C"-Homomorphinanの合成
- 戦後60年間の薬学教育の改革に関して薬学会、薬剤師会、病院薬剤師会、薬学教育協議会、文部科学省および厚生労働省が果たした役割の検証
- 総会講演 戦後60年間の薬学教育の改革に関して薬学会,薬剤師会,病院薬剤師会,薬学教育協議会,文部科学省および厚生労働省が果たした役割の検証
- Neue Pterosin-Derivate aus Pteris wallichiana AGARDH. und P. semipinnata L.
- 配位化合物の構造, 山田祥一郎著, A5版, 384頁, 4800円(化学同人)
- Addition of Molecular Fluorine to Azlactones : General Synthetic Method of erythro-β-Fluorinated α-Amino Acids
- Use of 1,3-Dioxin-4-ones and Related Compounds in Synthesis. XLIV. Asymmetric Aldol Reaction of 4-Trimethylsiloxy-6-methylene-1,3-dioxines : Use of Tartaric Acid-Derived (Acyloxy)borane Complex as the Catalyst
- Facile Synthesis of 5α-Fluorocholestan-3-one from 4-Cholesten-3-one via Molecular Fluorine Addition and Reductive Defluorination
- Use of 1,3-Dioxin-4-ones and Related Compounds in Sythesis. XXXVIII. Use of 1,3-Dioxin-4-ones Having a Fluorine or Trifluoromethyl Group at the 5-Position as _π2 Components in [2+2]-Photocycloaddition and Diels-Alder Reactions
- l-MENTHYL (2S)-2-PHENYL-3-(p-ANISYL)-(5Z)-BENZYLIDENE-4,6-DIOXO-1,3-OXAZINE-2-CARBOXYLATE : A NEW CHIRAL HETERODIENE AND MICHAEL ACCEPTOR
- Synthesis of 1,3-Dioxin-4-ones and Their Use in Synthesis XX. : (6S, 7S, 10R)- and (6R, 7S, 10R)-7-Isopropyl-10-mythyl-4-oxo-1,5-dioxaspiro[5.5]undec-2-enes; Synthesis and Their Use in Enantiomerically Pure Corey Lactone Analogue Synthesis
- Synthesis of 1,3-Dioxin-4-ones and Their Use in Synthesis. XVII. : Chiral Spirocyclic 4-Oxo-1,3-dioxin-5-carboxylates : Asymmetric Synthesis of Carbocyclic C-Nucleoside Precursors
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