AN EFFICIENT SYNTHESIS OF WF-3681, A NOVEL ALDOSE REDUCTASE INHIBITOR, AND ITS RELATED COMPOUNDS(Communications to the Editor)
スポンサーリンク
概要
- 論文の詳細を見る
WF-3681(1a), an aldose reductase inhibitor, and its related compounds(1b-1j) nave been synthesized by aldol condensation of phenylpyruvates and u-formylalkanoates as a key step.
- 公益社団法人日本薬学会の論文
- 1987-06-25
著者
-
鈴木 康隆
Exploratory Research Laboratories Fujisawa Pharmaceutical Co. Ltd.
-
奥 照夫
Exploratory reserch Laboratries, Fujisawa Pharmaceutical Co., Ltd.
-
奥 照夫
藤沢薬品探研
-
橋本 真志
Exploratory Research Laboratories Fujisawa Pharmaceutical Co. Ltd.
-
伊藤 義邦
Exploratory Research Laboratories, Fujisawa Pharmaceutical Co., Ltd.
-
沢田 弘造
Exploratory Research Laboratories Fujisawa Pharmaceutical Co. Ltd.
-
奥 照夫
Exploratory Reserch Laboratries Fujisawa Pharmaceutical Co. Ltd.
-
橋本 真志
Exploratory Research Laboratories Fujisativa Pharmaceutical Co. Ltd.
-
並木 隆之
Exploratory Research Laboratories, Fujisawa Pharmaceutical Co., Ltd.,
-
北浦 良彦
(Present address)Pfizer Central Research
-
北浦 良彦
Exploratory Research Laboratories, Fujisawa Pharmaceutical Co., Ltd.
-
伊藤 義邦
Exploratory Research Laboratories Fujisawa Pharmaceutical Co. Ltd.
-
並木 隆之
Exploratory Research Laboratories Fujisawa Pharmaceutical Co. Ltd.
関連論文
- Odorous Metabolites of Actinomyces Biwako-C and -D Strain isolated from the Bottom Deposits of Lake Biwa. Identification of Geosmin, 2-Methylisoborneol, and Furfural
- Synthesis of Kifunensine, an Immunomodulating Substrate Isolated from a Microbial Source
- 22 Kifunensineおよび8-epi-kifunensineの合成(口頭発表の部)
- 83(P69) 新規微小管作用物質WS9885B(ポスター発表の部)
- A New Metabolite from Pseudomonas pyrrolnitrica
- 2-(2-Heptenyl)-3-methyl-4-quinolinol from a Pseudomonas
- Oxypryrrolnitrin : A Metabolite of Pseudomonas
- STRUCTURE AND SYNTHESIS OF FK409,A NOVEL VASODILATOR ISOLATED FROM STREPTOMYCES AS A SEMI-ARTIFICIAL FERMENTATION PRODUCT
- 13 Amauroascus属菌の生産する降圧作用を有するアルカロイド WF6237の構造と合成
- STRUCTURE AND SYNTHESIS OF WB-3559 A, B, C AND D, NEW FIBRINOLYTIC AGENTS ISOLATED FROM FLAVOBACTERIUM sp.
- Synthesis and Aldose Reductase-Inhibitory Activities of Structural Analogues of WF-3681,a Novel Aldose Reductase Inhibitor
- Enantioselective Synthesis of Monocyclic β-Lactams Related to Nocardicins via a [2+2] Cycloaddition Reaction(Organic,Chemical)
- Preparation of 3-Aminonocardicinic Acid and Its Acyl Derivatives(Organic,Chemical)
- AN EFFICIENT SYNTHESIS OF WF-3681, A NOVEL ALDOSE REDUCTASE INHIBITOR, AND ITS RELATED COMPOUNDS(Communications to the Editor)
- 35 3-アザセファロスポリンの合成
- 43 ペニシリンよりModified β-lactam Antibioticsへの変換
- Synthesis of Some Polyhydroxylated Pyrrolidine Derivatives(Organic,Chemical)
- SYNTHESIS AND ADJUVANT ACTIVITY OF FK-156 ANALOGUES : ACYL DERIVATIVES OF N-[N^2-(L-ALANYL-γ-D-GLUTAMYL)-2 (L), 2'(D)-DIAMINO-1-PIMELOYL] GLYCINE
- Studies on Structure-Activity Relationships of FK-156,an Immunostimulating Peptide, and Related Compounds. II. Synthesis of N^2-(γ-D-Glutamyl)-2 (L), 2' (D)-diaminopimelic Acid as the Minimal Essential Structure of FK-156
- Studies on Structure-Activity Relationships of FK-156,an Immunostimulating Peptide, and Related Compounds. I. Synthesis of Stereoisomeric Analogues of FK-156
- SYNTHESIS AND IMMUNOSTIMULATING ACTIVITY OF FK-156 ANALOGUES : FATTY ACID DERIVATIVES OF N-[N^α-(γ-D-GLUTAMYL)-L-LYSYL]-D-ALANINE
- Studies on Phosphonic Acid Antibiotics. IV. Synthesis and Antibacterial Activity of Analogs of 3-(N-Acetyl-N-hydroxyamino)-propylphosphonic Acid (FR-900098)
- 76 免疫増強作用を有する微生物代謝産物Gludapcin(FK-156)の合成
- Studies on Phosphonic Acid Antibiotics. III. Structure and Synthesis of 3-(N-Acetyl-N-hydroxyamino) propylphosphonic Acid (FR-900098) and 3-(N-Acetyl-N-hydroxyamino)-2 (R)-hydroxypropyl-phosphonic Acid (FR-33289)
- Lithium Aluminum Hydride Partially Decomposed with (-)-N-Methylephedrine and 2-Alkylaminopyridine : An Improved Chiral Hydride Useful for the Practical Asymmetric Reduction of Achiral Cyclic Ketones
- Synthesis of Trilobine, Isotrilobine, and Obaberine
- Synthesis 8-epi-Kifunensine
- SYNTHESIS OF 8-EPI-KIFUNENSINE
- 最近のβ-ラクタム抗生物質の化学
- Hypocholesterolemic Alkaloids of Lentinus edodes (BERK.) SING. IV. Synthesis of Three Stereoisomers of Eritadenine
- Hypocholesterolemic Alkaloids of Lentinus edodes (BERK.) SING. III. Preparation of Analogous Compounds related to Eritadenine