多官能性化合物2- (N-シアノイミノ) チアゾリジン誘導体の合成化学的活用
スポンサーリンク
概要
- 論文の詳細を見る
- 有機合成化学協会の論文
- 1998-03-01
著者
-
田中 徹明
阪大院薬
-
田中 徹明
大阪大学薬学部製薬化学科
-
岩田 宙造
大阪大学薬学部製薬化学科
-
Tanaka T
Osaka Univ. Osaka Jpn
-
岩田 宙造
大阪大学薬学部
-
田中 恒雄
Department Of Pharmacy Hyogo College Of Medicine
-
田中 徹明
大阪大学薬学部
関連論文
- Synthetic Studies on Aphidicolane and Stemodane Diterpenes. IV.A Stereoselective Formal Total Synthesis of (±)-Aphidicolin
- Synthetic Studies on Aphidicolane and Stemodane Diterpenes. III.An Alternative Stereoselective Access to Aphidicolane-Type B/C/D-Ring System
- 61 アフィディコラン型およびステモダン型ジテルペンの合成研究(ポスター発表の部)
- Synthetic Studies on Aphidicolane and Stemodane Diterpenes. II. Neighboring Hydroxyl Group Participation in Stereoselective Syntheses of Tricyclo[6.3.1.0^]dodecanes Corresponding to the B/C/D-Ring Systems
- Synthetic Studies on Aphidicolane and Stemodane Diterpenes. I. Synthesis of (2'R^*, 4a'S^*, 8a'R^*)-2', 8a'-Dimethyl-4a', 5', 8', 8a'-tetrahydrospiro [2,5-cyclohexadiene-1,1'(2H)-naphthalene]-3'(4'H), 4,6' (7'H)-trione
- Synthetic Studies on Spiroketal Natural Products. V. Total Synthesis of (+)-Talaromycin A and (-)-talaromycin B
- Synthetic Studies on Spiroketal Natural Products. IV.A Stereoselective Synthesis of (3S, 5S, 6R, 9R, R_S)-3-Benzyloxymethyl-9-hydroxymethyl-5-(p-tolyl)sulfinyl-1,7-dioxaspiro[5.5]undecane, a Key Intermediate for Talaromycins
- Synthetic Studies on Spiroketal Natural Products. II. An Enantioselective Synthesis of (R)- and (S)-1,7-Dioxaspiro[5.5]undecane
- Synthetic Studies on Spiroketal Natural Products. I. : A Stereoselective Synthesis of (2R^*, 5R^*)- and (2R^*, 5S^*)-2-Methyl-1,6-dioxaspiro[4.5]decane
- Flavonol Glycosides in Leaves of Two Diospyros Species
- 102(P-59) (±)-Scopadulinの全合成(ポスター発表の部)
- 131(P-78) 抗腫瘍活性アセトゲニンMosin Bの不斉合成研究(ポスター発表の部)
- 多官能性化合物2- (N-シアノイミノ) チアゾリジン誘導体の合成化学的活用
- 50(P10) Macrocarpal類の不斉合成研究(ポスター発表の部)
- Synthetic Studies on Aphidicolane and Stemodane Diterpenes. V. A Facile Formal Total Synthesis of (±)-Aphidicolin via a Lewis Acid-Mediated Stereoselective Spiroannelation
- Lewis Acid-Mediated Stereoselective Spiroannelation : A Facile Access to Aphidicolane and Stemodane B/C/D Ring Systems
- P-18 (+)-Perhydrohistrionicotoxinの合成(ポスター発表の部)
- Synthetic Studies on Aromadendrane-Type Compounds. II.Stereoselective Synthesis of (+)-1,2-Didehydroaromadendrane
- Synthetic Studies on Aromadendrane-Type Compounds. I. Stereoselective Construction of Aromadendrane- and Alloaromadendrane-Type Skeletons
- Construction of Asymmetric Quaternary Carbon Center Containing Heteroatom via Regioselective Cleavage of Cyclopropane Ring Mediated by Mercury(II) Salt
- Synthetic Study on Gymnomitrol. II. A Synthesis of (±)-Isogymnomitrol
- 57 アロマデンドラン型化合物の不斉合成研究(ポスター発表の部)
- Synthetic Study on Gymnomitrol and Related Compounds. I.Preparation and Cyclopropane Ring Opening of 1,2,6-Trimethyltetracyclo[5.3.1.0^.0]undecan-9-one
- 7,7-Dimethyltricyclo[3.3.0.0^]octan-3-ones as Synthetic Intermediates. VI. An Improved Formal Synthesis of (±)-Descarboxyquadrone via Highly Regioselective Cyclopropane Ring Opening of Tricyclo[3.3.0.0^]octan-3-one
- 含窒素共役系の反応(第8報)Dimethyl Inidazole-4,5-dicarboxylateとAnetholeとの反応生成物の構造について
- 含窒素共役系の反応(第7報)N-CinnamylidenemethylamineとN-Methyl-maleimideとめ付加体について
- 含窒素共役系の反応(第6報)2,3-Diphenyl-5,6-dihydropyrazineとDiethyl FumarateまたはN-Methylmaleimideとの付加体の立体構造について
- 2-Oxo-1,2,3-oxathiazolidines. Its Application to Separation of Diastereoisomers of β-Amino-alcohols, 6-(4-Methoxy-2-piperidyl)-1,4-dioxaspiro [4,5] decan-6-ol and 2-Hydroxy-2-(2-piperidyl) cyclohexanone
- Synthetic Studies on Securitinine and Related Compounds. II. A Synthesis of 10a-Episecuritinine
- Synthetic Studies on Securitinine and Related Compounds. I. Stereochemistries of the Catalytic Hydrogenation Products of 6-(4-Methoxy-2-pyridyl)-1,4-dioxaspiro [4,5] decan-6-ol
- 93(P-22) 抗腫瘍活性アセトゲニン類の系統的不斉合成法の開発 : Murisolinの不斉合成への応用(ポスター発表の部)
- P-448 STRUCTURES OF STILBENE OLIGOMERS IN DIPTEROCARPACEAEOUS PLANTS
- New resveratrol oligomers in the stem bark of Vatica pauciflora
- Six New Heterocyclic Stilbene Oligomers from Stem Bark of Shorea hemsleyana.
- Five New Oligostilbenes with One or Two Dihydrofurans form the Stem Bark of Vatica rassak.
- A Novel Bridged Stilbenoid Trimer and Four Highly Condensed Stilbenoid Oligomers in Vatica rassak.
- Synthesis of 7-Thiaprostaglandin E_1 Congeners : Potent Inhibitors of Platelet Aggregation
- Synthesis of Thiaprostaglandin E_1 Derivatives
- SYNTHESIS OF NEW ANTINEOPLASTIC ALKYLIDENECYCLOPENTENONES
- SYNTHESIS OF NEW ANTINEOPLASTIC PROSTAGLANDINS
- TOTAL SYNTHESES OF STABLE PGI_2 DERIVATIVES : SYNTHESES OF 7-HYDROXY-AND 7-FLUORO-PGI_2
- Synthesis of New Secoprostaglandins as Inducers of Platelet Aggregation
- Platelet Anti-aggregant Activity of 2,2-Dimethylthiazolidine Hydrochloride and 2-(4-Hydroxy-3-methoxyphenyl)thiazolidine
- A New Synthesis of (±)-Agarospirol and (±)-Hinesol
- Synthetic Studies on Quadrone. I. An Approach to the Synthesis of (±)-Quadrone(Organic,Chemical)
- A FORMAL TOTAL SYNTHESIS OF (±)-QUADRONE
- Synthetic Studies on Acorane-Alaskane Sesquiterpenes. I. Total Synthesis of (±)-β-Acorenol
- 40 Acorane-Alaskane型セスキテルペンの合成研究
- Excellent Chiral Induction by Diene Iron-Tricarbonyl Moiety. I : Diastereoselective [4+2] Type Cycloaddition of 1-Azatriene Iron-Tricarbonyl Complex
- Melanogenesis Stimulation in Murine B16 Melanoma Cells by Kava (Piper methysticum) Rhizome Extract and Kavalactones(Pharmacognosy)
- A Modified Procedure for the Synthesis of Spirodienones from Phenolic α-Diazoketones
- Asymmetric Desymmetrization of Prochiral 1,3-Diols via Diastereoselective C-O Bond Fission of Bicyclic Acetal Using a Chiral Sulfoxide as a Chiral Auxiliary
- 4-(2-Aminoethylamino)-7H-benz[de]benzimidazo[2,1-a]isoquinoline-7-one as a Highly Sensitive Fluorescent LabelingReagent for Carnitine
- Antibacterial Activity of Stilbene Oligomers against Vancomycin-Resistant Enterococci (VRE) and Methicillin-Resistant Staphylococcus aureus (MRSA) and Their Synergism with Antibiotics
- A Monoterpene Glucoside and Three Megastigmane Glycosides from Juniperus communis var. depressa
- Stilbene Oligomers in Roots of Sophora moorcroftiana
- Stilbene Derivatives from Two Species of Gnetaceae
- Four New Glucosides of Stilbene Oligomers from theStem of Gnetum gnemonoides
- Stilbenoids in Lianas of Gnetum parvifolium
- Three New Trimeric Stilbenes from Gnetum gnemon
- Four New Glucosides of Stilbene Oligomers From the Stem of Gnetum gnemonoides.
- Inhibitory Effect of Plant Extracts on Production of Verotoxin by Enterohemorrhagic Escherichia coli 0157 : H7.
- スルフィニル基の特性を利用した新規合成反応の開発と天然物合成への応用
- SYNTHESIS OF NEW SULFUR-CONTAINING PROSTAGLANDIN I_1
- Revised Structure of Cercidinin A, a Novel Ellagitannin Having (R)-Hexahydroxydiphenoyl Esters at the 3, 4-Positions of Glucopyranose
- Synthetic Studies on Quadrone. II. Synthesis of Methyl (1R^*,3aR^*,6aR^*)-2,2-Dimethyl-2,3,3a,4,6,6a-hexahydro-1-(2-hydroxyethyl)-4-methylene-5-oxo-3a(1H)-pentaleneacetate, a Key Intermediate for the Synthesis of (±)-Quadrone(Organic,Chemical)
- Photolysis of Alkynyl(phenyl)iodonium Salts. Remarkable Solvent Effect and Generation of Acids
- Factors Affecting the Dissolution Rate of Sulpiride from Tablets Coated with Polyvinylacetal Diethylaminoacetate, a Gastric-Fluid-Soluble Polymer. II. Effect of Mechanical Destructive Force and Film Coating Strength in the Gastrointestinal Tract
- Potent NK_1 Receptor Antagonists : Synthesis and Antagonistic Activity of Various Heterocycles with an N-[3,5-Bis(trifluoromethyl)benzyl]-N-methylcarbamoyl Substituent
- Synthetic Studies on Spirovetivane Phytoalexins. III. : A Total Synthesis of (±)-Lubiminol
- Synthetic Studies on Spirovetivane Phytoalexins. II. : Stereoselective Synthesis of (2RS, 5RS, 6SR, 8RS, 10SR)-6-Hydroxymethyl-8-methoxymethoxy-10-methyl-2-pivaloyloxyspiro[4.5]decane
- Neighboring Hydroxyl Group Participation in Metal-Ammonia Reduction of Spirocyclic Dienones
- Synthetic Studies on Acorane-Alaskane Sesquiterpenes. II. : Total Synthesis of (±)-Acorenone
- 16 Spirovetivane型Phytoalexin類の合成研究 : (±)-Lubiminolおよび(±)-oxylubiminの立体選択的全合成
- Total Synthesis of (±)-α-Chamigrene and Brominated Chamigrene
- 38 スピロベチバン類の合成研究
- Resveratrol Tetramers with a C_6-C_3 or a C_1 Unit from Upuna borneensis
- Resveratrol Oligomers and Their O-Glucosides from Cotylelobium lanceolatum
- A New and Known Cytotoxic Aryltetralin-Type Lignans from Stems of Bursera graveolens
- Resveratrol Derivatives from Upuna borneensis
- Three New Trimeric Stilbenes from Gnetum gnemon.
- Six Flavonostilbenes from Gnetum africanum and Gnetum gnemon
- 7,7-Dimethyltricyclo[3.3.0.0^]octan-r-ones as Synthetic Intermediates. V. : An Improved Synthesis of (±)-Pentalenene
- 7,7-Dimethyltricyclo[3.3.0.0^]octan-3-ones as Synthetic Intermediates. IV. : A Further Examination of Cyclopropane Ring Opening in the Tricyclo[3.3.0.0^]octan-3-one System
- Inhibition of Preadipocyte Differentiation by Germacranolides from Calea urticifolia in 3T3-L1 Cells
- Antioxidant Activity of Hydroxyflavonoids
- An Approach to the Stereoselective Synthesis of Nidifocene. II.Total Synthesis of (±)-Dehalogenonidefocene
- 43(PA1-1) カミグラン型セスキテルペン類の合成研究(ポスター発表の部)
- 7,7-Dimethyltricyclo[3.3.0.0.^]octan-3-ones as Synthetic Intermediates. I. : Preparation and Cyclopropane Ring Opening of 7,7-Dimethyl-5-(2-propenyl)tricyclo[3.3.0.0^]octan-3-one
- Stereochemistry of the Intramolecular Cyclization Products of Methyl 2-Bromo-5-(4-hydroxyphenyl) hexanoate : Synthesis of trans- and cis-1,4-Dimethyltetralin
- Photochemical Oxidation. II. Biogenetic-Type Conversion of Ligularol and Furanoeremophilane into 6β-Hydroxyeremophilenolide and Eremophilenolide
- An Approach to the Stereoselective Synthesis of Nidifocene. III.Total Syntheses of the Stereoisomers of (±)-Nidifocene from(±)-Dehalogenonidifocene
- 11 ハロカミグラン型セスキテルペン類縁体の合成研究(ポスター発表の部)
- An Approach to the Stereoselective Synthesis of Nidifocene : Regio- and Stereoselective Synthesis of vic-trans-Bromochlorocyclohexane Ring System
- Synthesis of Four Possible Isomers of 9-(Bromomethylene)-1,2,5-trimethylspiro[5.5]undeca-1,7-dien-3-one : Structure Elucidation of a Brominated Rearranged Chamigrane-Type Sesquiterpene
- 7,7-Dimethyltricyclo[3.3.0.0^]octan-3-ones as Synthetic Intermediates. III. : Total Synthesis of (±)-Descarboxyquadrone
- 7,7-Dimethyltricyclo[3.3.0.0^]octan-3-ones as Synthetic Intermediates. II. : A Total Synthesis of (±)-Pentalenene, an Angular Triquinane Sesquiterpene
- 45 Tricyclo[3.3.0.0^]octan-3-one化合物を鍵中間体とするポリキナン型セスキテルペン類の合成研究 : (±)-Pentalenene及び(±)-Quadroneの全合成
- TOTAL SYNTHESIS OF (±)-PENTALENENE
- 2 クロロスルホリピッドの不斉全合成(口頭発表の部)