SYNTHESES OF THE TETRAHYDROFURAN SUBUNITS OF TETRONASIN AND TETRONOMYCIN
スポンサーリンク
概要
- 論文の詳細を見る
L-Rhamnal has been transformed into the tetrahydrofuran subunits (14 and 21) of tetronasin (ICI-139603) (1) and tetronomycin (2), in which the three chiral centers at the 2- and 5-positions and the methoxy-bearing carbon are of mirror image.
- 公益社団法人日本薬学会の論文
- 1990-06-25
著者
-
野村 敬一
Faculty of Pharmaceutical Sciences, Toyama Medical Pharmaceutical University
-
野村 敬一
Faculty Of Pharmaceutical Sciences Toyama Medical And Pharmaceutical University
-
吉井 英一
Faculty Of Pharmaceutical Sciences Toyama Medical And Pharmaceutical University
-
吉井 英一
富山医科薬科大学薬学部
-
堀 耕造
Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University
-
数野 秀樹
Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University
-
数野 秀樹
Faculty Of Pharmaceutical Sciences Toyama Medical And Pharmaceutical University
-
堀 耕造
Faculty Of Pharmaceutical Sciences Toyama Medical And Pharmaceutical University
関連論文
- Studies on Mesoionic Compounds. XII. Synthesis of 1,2,3-Thiadiazolium-4-aminide Derivatives and Their Characterization
- PREPARATION OPTICALLY ACTIVE α, β-UNSATURATED PHOSPHONATES AND SULFOXIDES FROM PHENYLSULFENYLMETHANEPHOSPHONATES
- CHIRAL PHENYLSULFENYLMETHANEPHOSPHONIC ESTERS, THEIR PREPARATIONS AND ABSOLUTE CONFIGURATIONS
- Intramolecular Diels-Alder Reaction of Undeca-2,8,10-trienoate
- Optically Active Alkyl Phenyl Phosphoramidates : Preparation and Stereochemistry of Acid-catalyzed Alcoholysis
- 8,13-Diazagona-1,3,5 (10)-triene-12-ones, Synthesis and Stereochemistry
- N-モノ置換Diphenylphosphinamide類のアルキル化反応
- Studies on the Synthesis of Cardiotonic Steroids. III. New and Effective Route to Bufadienolides
- Selective Reduction of Conjugated Enones and Dienones with Trialkylsilane and Titanium Tetrachloride
- Studies on the Synthesis of Cardiotonic Steroids. II. Synthesis of 17β-(3-Furyl)-5β, 14β-androstane-3β, 14β-diol
- α-Chlorinative Homologation of α, β-Unsaturated Esters
- Acid-Catalyzed Methanolysis of optically Active N-Cyclohexyl Methylphenyl-phosphinamide : A Stereochemical Evidence for A-2 Mechanism
- Studies on the Synthesis of Cardiotonic Steroids. I. Efficient Synthesis of Cardenolides
- Studies on Mesoionic Compounds. XIV. Synthesis of Mesoionic 1,3-Thiazolium-4-thiolates
- Studies on Mesoionic Compounds. XIII. Synthesis of Mesoionic 1,2,3-Thiadiazolium-4-thiolates
- Studies on Mesoionic Compounds. IX. Synthesis of Bicyclic Mesoionic Compounds
- Studies on Mesoionic Compounds. VIII. Some Reactions of the Mesoionic 4-Amino-1,2,4-triazolium-3-thiolate System
- Studies on Mesoionic Compounds. V. Synthesis and Cycloaddition Reaction of anhydro-5-Hydroxy-1,3-oxathiolium Hydroxide System
- Introduction of a 3-Alkoxycarbonyl-2-propenyl Group at the ortho Position of Phenol and Naphthol via α-Aryloxy-γ-butyrolactone. Application to Syntheses of (±)-Nanaomycin A and a 1-Anthracenone
- Syntheses of 5,6-Benzo- and 5,6-Naphtho-(1R, 3R, 4S, 8R)-4,8-dihydroxy-3-methyl-2-oxabicyclo [2.2.2] oct-5-ene Derivatives
- Synthesis and Optical Resolution of 4,6-Dideoxy-3,5-O-isopropylidene-2-O-(methoxymethyl)-DL-glucitol
- SYNTHESIS OF THE B/C-RING SYSTEM OF TETRONASIN (ICI-139603)
- SYNTHESIS OF THE POLYETHER FRAGMENT A/B-RING SYSTEM OF TETRONOMYCIN
- SYNTHESES OF THE TETRAHYDROFURAN SUBUNITS OF TETRONASIN AND TETRONOMYCIN
- AN EFFICIENT 3(C)-ACYLATION OF TETRAMIC ACIDS INVOLVING ACYL MIGRATION OF 4(O)-ACYLATES(Communications to the Editor)
- AN EFFICIENT METHOD FOR 3(C)-ACYLATION OF TETRONIC ACIDS(Communications to the Editor)
- Cyanophthalide Annulation with 4-(5-Alkoxy-2-furyl)-3-buten-2-one. Application to the Synthesis of a (Naphtho)pyrano-γ-lactone
- Heteroaromatic Analogs of Benzomorphan. III. Synthesis of 1,2,3,4,5,6-Hexahydro-2,6-methano-3-methylpyrido [3,2-d] azocine
- Heteroaromatic Analogs of Benzomorphan. II. Synthesis of 2-Azabicyclo-[3.3.1] nonane Derivatives fused to Pyridine Ring. (2)
- Reaction of Conjugated Dienones with Hydrazoic Acid. II.
- Tetrahydronaphthylamines and Related Compounds. III. Synthesis of 1,2,3,4-Tetrahydro-2-naphthylamine and 6-Amino-5,6,7,8-tetrahydroquinoline Derivatives
- Synthesis of 1,2,3,4,5,6-Hexahydro-1,5-methano-2-methylpyrido [2,3-c] azocine
- エノールエーテルと窒化水素酸との反応
- 71 (±)-24-O-Methylchlorothricolideの合成(ポスター発表の部)
- The Reaction of Enamines derived from Cyclic Ketones with Methyl Tetrolate. A New Synthesis of rac-Muscone
- Synthesis of Purpnigenin
- 米国産NTU頁岩油成分の研究(第10報)コロラド産頁岩油の軽油留分より(+)-Drim-8-eneの検出
- 2-Phenoxy-benzoxazaphosphole-2-oxide, a Novel Phosphorylating Agent of Alcohols
- Facile Preparation of Pregn-14-ene-20,21-diones
- Hydrosilation of α, β-Unsaturated Esters
- A Convenient Method for the Preparation of Alkyl Phenyl Phosphates
- Reduction of Mixed Carboxylic-Diphenylphosphoric Anhydrides with Sodium Borohydride
- The Reaction of o-Phenylenediamine with Phenyl Phosphorodichloridate. Synthesis and Reactions of 2-Phenoxy-1,3-dihydro-2H-1,3,2-benzodiazaphosphole-2-oxide and Related Compounds
- Pregn-14-en-20-ones : Facile Preparation and 14β-Hydroxylation
- Synthesis of Xysmalogenin
- 72 Tetronolideの合成研究
- TRIETHYLSILYLATION OF HYDROXYL GROUPS WITH A KETENE TRIETHYLSILYL ACETAL 2-METHYL-1-TRIETHYLSILYLOXY-1-METHOXYPROPENE
- ジキナンおよびトリキナン型セスキテルペンの合成
- Syntheses of Methyl α-and β-DL-Tetronitrosides (or Kijanosides)
- 2-Ethylenedioxy-7-azabicyclo[4.1.0]heptaneの合成と加水分解反応
- Tetrahydronaphthylamines and Related Compounds. II. Synthesis of 1,2,3,4-Tetrahydro-6,7-dimethoxy-2-phenyl-2-naphthylamine
- Syntheses of 1,2,3,4-Tetrahydro-2-naphthylamine Derivatives
- ラクトン環を有する生物活性天然物の合成.強心性ステロイド, ナフトキノン系抗生物質, 及びテトロン酸系イオノフォア抗生物質
- テトロン酸系生物活性天然物の合成
- 日本薬学会教育賞受賞 山崎高應先生の業績
- ピラノ・ナフトキノン系抗生物質の合成
- ピラノ・ナフトキノン系抗生物質の合成研究
- 動物性生薬の品質評価に関する研究(第2報)ジャコウの品質評価に関する研究
- The Reaction of α, β-Unsaturated Ketones with Azides. III.
- ピラノ・ナフトキノン系抗生物質の合成
- ジキナンおよびトリキナン型セスキテルペンの合成
- 懇親会は総会前日に役員等で, ミキサーは予約参加を(年会懇親会のあり方)
- Study on the Components of Musk. I. Ether Soluble Components
- Reaction of Conjugated Dienones with Hydrazoic Acid
- The Reaction of α, β-Unsaturated Cycloalkenones with Azides. I. The Anomalous Products in the Schmidt Reaction