Structure and Synthesis of Acid A, an Oxidation Product of Lycoramine

スポンサーリンク

概要

• 論文の詳細を見る

• The structure of acid A, an oxidation product of lycoramine (1), an Ameryllidaceae alkaloid, was established as 4 on the basis of spectral and chemical evidence. The racemic methyl ester (8) of acid A (4) was synthesized.

• 社団法人日本薬学会の論文
• 1986-06-25

著者

• 小林 茂

  Faculty Of Home Economics Shikoku University

• 飯塚 欣二

  Central Research Laboratories, Kissei Pharmaceutical Co., Ltd.,

• 飯塚 欣二

  Central Research Laboratories Kissei Pharmaceutical Co. Ltd.

• 入江 寛

  Faculty of Pharmaceutical Sciences, Nagasaki University

• 入江 寛

  Faculty Of Pharmaceutical Sciences Kyoto University

• 徳元 俊弘

  Faculty of Pharmaceutical Sciences, Tokushima University

• 上尾 庄次郎

  Faculty of Pharmaceutical Sciences, Kobe Gakuin University

• 小池(旧姓太田) 知三

  Faculty of Pharmaceutical Sciences, Tokushima University

• 飯塚 欣二

  Faculty of Pharmaceutical Sciences, Kyoto University

• 上尾 庄次郎

  Faculty Of Pharmaceutical Sciences Kobe Gakuin University

• 小池(旧姓太田) 知三

  Faculty Of Pharmaceutical Sciences Tokushima University

• 徳元 俊弘

  Faculty Of Pharmaceutical Sciences Tokushima University

関連論文

• Synthesis of Human Renin Inhibitory Peptides, Angiotensinogen Transition-State Analogs Containing a Retro-Inverso Amide Bond
• Synthesis and Structure-Activity Relationships of Human Renin Inhibitors Designed from Angiotensinogen Transition State
• A SIMPLE DIASTEREOSELECTIVE SYNTHESIS OF CYCLOHEXYLNORSTATINE AND ALLOCYCLOHEXYLNORSTATINE
• Synthesis of a Germination Self-Inhibitor, (-)-Gloeosporone, and Related Compounds and Evaluation of Their Activities
• Synthesis of Amaryllidaceae Alkaloids, (±)-Cherylline and (±)-Latifine
• カニクイザルにおけるクロドロネート(KCO-692)の卵巣摘出骨粗鬆症モデルに対する効果
• Studies on Peptides. LXXIX. : By-Products derived from N^α-Protected Tryptophan by Acids
• Studies on Peptides. LXXIII. Examination of the Methanesulphonic Acid Procedure for the Synthesis of Peptides containing Methionine
• Studies on the Structure-Toxicity Relationship of AK-Toxin, a Host-Specific Toxin to Japanese White Pear, Produced by Alternaria kikuchiana : Synthesis of Methyl (4S, 5R)-4-(N-Acetylphenylalanyl)oxy-5,6-epoxy-5-methylhex-2(E)-enoate and Its Stereoisomers
• Synthesis of 5,6,7,8-Tetrahydroquinolines by Thermolysis of Oxime O-Allyl Ethers in the Presence of Boron Trifluoride Etherate
• Synthesis of the Simple Macrolides, Patulolide A and Patulolide C
• Cyclopentenone Annulation of 1,4-Diketones with Potassium Phosphate Tribasic : A Synthesis of a Monoterpene Alkaloid, (±)-Tecomanine
• A Synthesis of (-)-Bursatellin
• Synthesis of Methyl Esters of AF-Toxin IIa and IIc, Toxins to Japanese White Pear Produced by Alternaria alternata Strawberry Pathotype
• Synthesis of (-)-Patchoulipyridine and Related Compounds
• Synthesis of (±)-Heritol, a Sesquiterpene Lactone belonging to the Aromatic Cadinane Group
• Synthesis of the Methyl Ester of AK-Toxin II, a Host-Specific Toxin to Japanese white Pear, and Its Congeners : : Structure-Toxicity Relationship of the Toxin
• α-アドレナリン遮断作用を有するアボガランタミン類似体の合成(第7報)2-Iodo-N-(2-iodobenzyl)-β-phenethylamineの光化学閉環
• α-アドレナリン遮断作用を有するアポガランタミン類似体の合成(第4報)光化学閉環による合成その2
• Structure-Activity Relationship of Fluorine-Containing Renin Inhibitory Peptides Based upon the Tertiary Structure of Human Renin
• NEW HUMAN RENIN INHIBITORY PEPTIDES : ANGIOTENSINOGEN TRANSITION-STATE ANALOGUES CONTAINING NOVEL LEU-VAL REPLACEMENT AND A RETRO-INVERSO AMIDE BOND
• TOTAL SYNTHESIS OP ESTERS OP AK-TOXIN II AND AF-TOXIN IIC STARTING FROM VITAMIN C AS A CHIRAL MATERIAL(Communications to the Editor)
• SYNTHESIS OF THE HOST-SPECIFIC TOXINS AF-TOXIN II_C AND AK-TOXIN CONGENERS AND THEIR STEREOSTRUCTURE-TOXICITY RELATIONSHIP
• Alkaloidal Constituents of Leucojum autumnale L. (Amaryllidaceae)
• Regioselective Cleavage Reaction of the Aromatic Methylenedioxy Ring. VI. Synthesis of Phenothiazine Analogues by Using the Cleavage Reaction with Sodium Methoxide-Thiols in Dimethyl Sulfoxide and Evaluation of Their Biological Activities
• Isolation and Structure Elucidation of a Novel Alkaloid, Incartine, a Supposed Biosynthetic Intermediate, from Flowers of Lycoris incarnata
• Regioselective cleavage Reaction of the Aromatic methylenedioxy Ring. V. Cleavage with Sodium Alkoxides-Alcohols, Potassium tert-Butoxide-Alcohols, Dimsyl Anion-Methyl Alcohol, Metallic Sodium-Alcohols, and Sodium Cyanide in Dipolar Aprotic Solvents
• Alkaloidal Constituents of the Flowers of Lycoris radiata HERB. : Amaryllidaceae
• Synthesis of Apogalanthamine Analogues as α-Adrenergic Blocking Agents. XIII. Syntheses of Phenolic 8-Hydroxy-5,6,7,8-tetrahydrodibenz[c, e]azocines
• Syntheses of Apogalanthamine Analogues as α-Adrenergic Blocking Agents. XII. : Syntheses and Stereochemistry of Methoxy and Methylenedioxy Derivatives of 8-Hydroxy-5,6,7,8-tetrahydrodibenz-[c, e]azocines
• Alkaloidal Constituents of Hymenocallis rotata HERB. (Amaryllidaceae)(Organic,Chemical)
• Structures of Acid B and Related Compounds, Oxidation Products of Lycoramine
• Structure and Synthesis of Acid A, an Oxidation Product of Lycoramine
• Iridoid Glucosides from Lamium amplexicaule
• Alkaloidal Constituents of Leucojum asetivum L. (Amaryllidaceae)
• Studies on Constituents of Bignoniaceae Plants. IV. Isolation and Structure of a New Iridoid Glucoside, Campsiside, from Campsis chinensis
• Syntheses of Apogalanthamine Analogs as α-Adrenergic Blocking Agents. VIII. Syntheses of 4- and 9-Bromo-5,6,7,8-tetrahydrodibenz [c, e] azocines and Their Methylenedioxy Derivatives
• Alkaloidal Constituents of Crinum latifolium and Crinum bulbispermum (Amaryllidaceae)
• ANTIFEEDANTS FOR THE LARVAE OF THE YELLOW BUTTERFLY, EUREMA BECABE MANDARINA, IN LYCORIS RADIATA
• Cleavage of the Methylenedioxy Ring. III. Cleavage with Sodium Benzyloxide in Dimethyl Sulfoxide
• Isolation of O-Demethyllycoramine from Bulbs of Lycoris radiata HERB.
• Transformation of Tazettine to Pretazettine
• 四年生の講座配属について(四年生の講座配属)
• SYNTHESIS OF BICYCLO [4. 3. 0] NONENONE AND BICYCLO [3. 3. 0] OCTENONE DERIVATIVES BY INTRAMOLECULAR WADSWORTH-EMMONS REACTION : FORMAL SYNTHESIS OF THE SESQUITERPENE CEDRENE
• Synthesis of Methoxyonychine and Use of ^1H- and ^C-Nuclear Magnetic Resonance Spectra for Structure Determination of Geometrical Isomers of Indan-1-one Oxime Derivatives
• Thermolysis of Oxime O-Allyl Ethers : A New Method for Pyridine Synthesis
• Synthesis of the Alkaloid, Xylopinine and the Related Compound by Photo-induced Rearrangement of Spiroisoquinoline
• 5 (±)-Lycoramineの全合成
• Alkaloids of the Amaryllidaceae. A New Alkaloid, Sanguinine, from Lycoris sanguinea MAXIM. var. Kiushiana MAKINO, and Pretazettine from Lycoris radiata HERB.
• ビスデヒドロジヒドロエンメインの熱分解物の合成 : 第1報 6-Hydroxy-7-methylphthalideおよび2-Hydroxymethyl-6,6-dimethyl-5-oxo-1-cyclohexenecarboxylic Acid Lactoneの合成
• エンメインの構造に関する化学的研究
• Galanthamine Chemistry. V. Formation of Hydroxyapogalanthamine from Galanthaminone and the Synthesis of its Trimethyl Ether.
• An Improved Synthesis of N-(Butylaminocarbonyl)-4-hydroxymethyl-benzenesulfonamide, One of the Metabolites of Tolbutamide, and Synthesis of Its Formyl Derivative
• ジヒドロリコリンの合成
• Fumariline型塩基のマススペクトルについて(第1報)C環上のアルコオキシ基の位置とそのマススペクトルの関係および中間体法を用いた開裂機構
• 1,2,3,6-Tetrahydro-6-(3,4-dimethoxyphenyl)-phthalic Acidおよび関連化合物のFriedel-Crafts反応について
• Dimethoxyindanone類のマススペクトルについて
• Isolation and Characterization of 10,11-Dihydroatlantone and Related Compounds from Ginkgo biloba L.
• 36 (±)-Clivonineおよび(±)-Clividineの合成研究
• X-Ray Crystallographic Determination of the Structure of the Alkaloid Protostemonine
• シラネアオイの根茎の成分研究(第2報) : Glaupalolの全合成
• 22 Dihydrolycorineの合成
• ハマウド根の成分 : その6 Hamaudolの絶対配置について
• 31 (±)-Ochotensine及び類似化合物の全合成
• ハマウド根の成分 その5 : 5,7-Dimethoxy-3-hydroxy-2,2-dimethyl-chromanのJones酸化反応成績体について
• シラネアオイの根茎の成分研究(第1報) : Glaupalolの構造について
• イチョウ心材成分の研究(第5報) : Bilobanoneの構造と絶対配置について
• The Structure of Stenine, a New Alkaloid Occurring in Stemona Tuberosa
• The structure of the Rearrangement Product obtained by a Prevost-Woodward Reaction on 14-Hydroxydeoxydihydrocodeine Methine
• A Synthesis of Tetrahydrooxocrinine Methine
• 1-Substituted Imidazoles as Useful Catalysts for Acylation of Alcohols
• An Improved and Convenient Procedure for the Synthesis of 1-Substituted Imidazoles
• 1-ACYL-3-SUBSTITUTED IMIDAZOLIUM SALTS AS HIGHLY REACTIVE ACYLATING AGENTS
• Studies on Peptides. LXXIV. Convenient Procedure for the Preparation of Methionine Sulphoxide Derivatives
• AN APPROACH TO A SYNTHESIS OF THE HOST-SPECIFIC TOXINS AK-TOXIN I AND II, STARTING FROM VITAMIN C AS A CHIRAL MATERIAL
• An Improved and Convenient Synthesis of Esters Using 1,1'-Carbonyldiimidazole and a Reactive Halide
• A Useful Reagent for the Beckmann Rearrangement and the Synthesis of Nitriles from Carboxamides : N, N'-Carbonyldiimidazole and Reactive Halides
• A NOVEL ONE STEP CONVERSION OF ALCOHOLS INTO ALKYL BROMIDES OR IODIDES
• Photochemical Syntheses of Apogalanthamine Analogs as α-Adrenergic Blocking Agents
• Syntheses of Apogalanthamine Analogs as α-Adrenergic Blocking Agents
• ジフェン酸モノメチルエステル誘導体の合成 その2
• Studies on the α-Adrenolytic Activities of Apogalanthamine Analogs
• 2′-Bromomethyl-2-biphenylcarbaldehydeとシアン化ナトリウムとの反応
• Synthesis of 6-(β-Bromoethyl)-10,11-methylenedioxy-5,6,7,8-tetrahydrodibenz-[c, e]azocine (DA-VIII-MBr) as a New Specific α-Adrenergic Blocking Agent
• Synthesis of 2'-Cyanomethyl-2-biphenylcarboxylic Acid
• Studies on the Syntheses of Benzoheterocyclic Compounds. VI. Diphenide and Its Methoxyl Derivatives
• Lycoris Alkaloids. XXIV. : Isolation and Characterization of Lycoremine.
• 駆虫薬の合成研究 第6・7報
• Studies on Peptides. XCVI. Behavior of S-Acetamidomethylcysteine Sulfoxide under Deprotecting Conditions in Peptide Synthesis
• Studies on Peptides. LXXXIII. Behavior of S-Substituted Cysteine Sulfoxides under Deprotecting Conditions in Peptide Synthesis
• Behaviour of S-Substituted Cysteine Sulfoxide under Acidolytical Deprotecting Conditions
• Studies on Peptides. L. Acidolysis of Protecting Groups in Peptide Chemistry by Fluorosulphonic Acid and Methanesulphonic Acid
• ハロゲン置換N-Benzyl-β-phenethylamine誘導体の光化学反応について
• Syntheses of Apogalanthamine Analogs as α-Adrenergic Blocking Agents. III. 5,6,7,8-Tetrahydrodibenz [c, e] azocine and Its 6-Substituted Derivatives
• Syntheses of Methylenedioxydiphenides and Dimethoxydiphenides
• Synthesis of optically Active Deoxytazettine Neomethine
• Cleavage of the Methylenedioxy Ring. II. Cleavage with Sodium Phenoxide and Methoxide in Dimethyl Sulfoxide
• Cleavage of the Methylenedioxy Group with Sodium Methoxide in Dimethyl Sulfoxide
• Alpha-adrenolytic Activities of N-Benzyl-β-phenethylamine Derivatives on Isolated Smooth Muscles

もっと見る 閉じる

スポンサーリンク