Synthesis of Southern (C1'-C11') and Eastern (C8-C18) Fragments of Pamamycin-607, an Aerial Mycelium-inducing Substance of Streptomyces alboniger(Organic Chemistry)
スポンサーリンク
概要
- 論文の詳細を見る
Synthesis of the southern C1'-C11' and eastern C8-C18 fragments of pamamycin-607, an aerial mycelium-inducing substance of Streptomyces alboniger, was achieved. The southern fragment was synthesized by using the Evans aldol reaction and cis-selective iodoetherification as the key steps in a 9.6% overall yield (7 steps). The eastern fragment was constructed via the Julia coupling reaction and cis-selective iodoetherification in a 3.0% overall yield (8 steps from the known epoxide).
- 社団法人日本農芸化学会の論文
- 2001-12-23
著者
-
Kuwahara Shigefumi
Laboratory Of Agricultural Chemicals Faculty Of Agriculture Ibaraki University
-
Kiyota Hiromasa
Laboratory Of Applied Bioorganic Chemistry Division Of Bioscience & Biotechnology For Future Bio
-
Oritani Takayuki
Laboratory Of Applied Bioorganic Chemistry Division Of Life Science Graduate School Of Agricultural
-
FURUYA Yukito
Laboratory of Applied Bioorganic Chemistry, Division of Life Science, Graduate School of Agricultura
-
Furuya Yukito
Laboratory Of Applied Bioorganic Chemistry Division Of Life Science Graduate School Of Agricultural
-
Kiyota Hiromasa
Laboratory Of Applied Bioorganic Chemistry Division Of Life Science Graduate School Of Agricultural
-
Oritani Takayuki
Laboratory Of Applied Bioorganic Chemistry Division Of Life Science Graduate School Of Agricultural
-
Kuwahara Shigefumi
Laboratory Of Applied Bioorganic Chemistry Division Of Life Science Graduate School Of Agricultural
関連論文
- Synthesis of Both Enantiomers of 15-Hexadecanolide, a Sex Pheromone Component of the Stink Bug, Piezodorus hybneri
- Synthesis of an Antifungal Naphthoquinone Isolated from Rhinacanthus nasutus (Acanthaceae)
- Synthesis of (±)-Methyl Tuberonate, a Potato Tuber-forming Substance, and Its Epimer
- Four Novel Pseudoalkaloid Taxanes from the Seeds of the Chinese Yew, Taxus chinensis var. mairei
- Synthesis and Absolute Configuration of a Cytotoxic Fatty Acid Isolated from the Mushroom, Hericium erinaceum
- Synthesis of an Antifungal Naphthopyran Derivative Isolated from Rhinacanthus nasutus (Acanthaceae)(Organic Chemistry)
- Hydrolysis of S-2-Aminoethylcysteinyl Peptide Bond by Achromobacter Protease I
- Synthesis of All Four Possible Stereoisomers of 5,9-Dimethylpentadecane, the Major Sex Pheromone Component of the Coffee Leaf Miner Moth, Perileucoptera coffeella
- Preparation of (-)-Periplanone D and Its Physical and Spectroscopic Properties
- Effects of γ-Terpinene on Lipid Concentrations in Serum Using Triton WR1339-Treated Rats(Food & Nutrition Sience)
- Antioxidative Effect of Citrus Essential Oil Components on Human Low-density Lipoprotein In Vitro(Food & Nutrition Science)
- Enantioselective Total Synthesis of Enokipodins A-D, Antimicrobial Sesquiterpenes Produced by the Mushroom, Flammulina velutipes
- New 2(3→20)Abeotaxane and 3, 11-Cyclotaxane from Needles of Taxus cuspidata
- Novel Bicyclic Taxane Diterpenoids from the Needles of Chinese Yew, Taxus Mairei
- Polyoxygenated Cyclohexenes from the Chinese Tree, Uvaria Purpurea(Organic Chemistry)
- Four Polyoxygenated Cyclohexenes from the Chinese Tree, Uvaria Purpurea
- Four Novel Taxane Diterpenoids from the Needles of Japanese Yew, Taxus cuspidata
- Isolation and Structural Determination of a Novel Bicyclic Taxane Diterpene from Needles of the Chinese Yew, Taxus mairei
- A Newly Rearranged 2(3→20) Abeotaxane Diterpene from the Bark o Chinese Yew, Taxus mairei
- Synthesis of Robinal, a Highly Conjugated Monoterpenoid from the Mite, Rhizoglyphus robini
- Two Novel Taxane Diterpenoids From the Needles of Japanese Yew, Taxus Cuspidata
- Synthesis of the Sex Pheromone of the Citrus Mealybug, Pseudococcus cryptus(Organic Chemistry)
- Two New Alkaloidal Taxoids from the Needles of Taxus canadensis
- Inhibitory Activity of (9R,10S,12Z)-9,10-Dihydroxy-8-oxo-octadecenoic Acid, Its C-9 Epimer and Their Derivatives toward the Growth of Tea Pollen Tubes
- Synthesis of the (17R)- and (17S)-Isomers of Volicitin, an Elicitor of Plant Volatiles Contained in the Oral Secretion of the Beet Armyworm(Organic Chemistry)
- Simple Synthesis of 5,9-Dimethylated Long-Chain Alkanes, the Sex Pheromones of Leaf Miner Moths
- Simple Synthesis of the Major Sex Pheromone Components of Drosophila ananassae and D. pallidosa
- Synthesis of the Racemate of (Z)-exo-α-Bergamotenal, a Pheromone Component of the White-spotted Spined Bug, Eysarcoris parvus Uhler(Organic Chemistry)
- Synthesis of (R, Z)-7, 15-Hexadecadien-4-olide, the Sex Pheromone of the Yellowish Elongate Chafer (Heptophylla picea)
- A Novel Rearranged Taxoid from Needles of the Japanese Yew, Taxus cuspidata Sieb. et Zucc.
- New Taxane Diterpenoid from Seed of the Chinese Yew, Taxus yunnanensis
- Synthesis of Naturally Derived Bioactive Compounds of Agricultural Interest
- Synthesis of Macrotetrolide α, a Designed Polynactin Analog Composed of (+)- and (-)-Bishomononactic Acids(Organic Chemistry)
- Enantioselective Synthesis of the (1S,5R)-Enantiomer of Litseaverticillols A and B
- Synthesis of Southern (C1'-C11') and Eastern (C8-C18) Fragments of Pamamycin-607, an Aerial Mycelium-inducing Substance of Streptomyces alboniger(Organic Chemistry)
- Synthesis of (-)-Methyl Shikimate via Enzymatic Resolution of (1S^*, 4R^*, 5R^*)-4-Hydroxy-6-oxabicyclo [3.2.1] oct-2-en-7-one(Organic Chemistry)
- New 11 (15→1) Abeotaxane, 11 (15→1), 11 (10→9) Bisabeotaxane and 3,11-Cyclotaxanes from Taxus yunnanensis
- Enzymatic Resolution of (±)-Epoxy-β-cyclogeraniol, a Synthetic Precursor for Abscisic Acid Analogs
- Total Synthesis of Natural Products of Microbial Origins(Recent Topics of the Agricultunal Biological Science in Tohoku University)
- Microbial Hydroxylation of (±)- and(-)-(2Z, 4E)-5-(1', 2'-Epoxy-2', 6', 6'-trimethylcyclohexyl)-3-methyl-2,4-pentadienoic acid into (±)-and (-)-Xanthoxin Acid by Cunninghamella echinulata
- Synthesis of Both Enantiomers of Isorobinal, a Novel Cyclic Monoterpene Isolated from the Astigmatid Mite, Rhizoglyphus sp.(Organic Chemistry)
- Synthesis of (±)-Methyl Bishomononactate, a Monomeric Component of Polynactin Antibiotics
- Preparation of N-Substituted Aryl and Alkyl Carbamates and Their Inhibitory Effect on Oat Seed Germination(Organic Chemistry)
- Phytochemical Study on the Constitution of the Bark of Chinese Yew, Taxus Mairei
- A Concise Synthetic Approach to β,γ-Dehydrocurvularin : Synthesis of (±)-Di-O-Methyl-β,γ-dehydrocurvularin
- Enantioselective Synthesis and Stereochemical Revision of Communiols A-C, Antibacterial 2,4-Disubstituted Tetrahydrofurans from the Coprophilous Fungus Podospora communis
- Partial Racemization Occurring in the Hydroxylactonization of a δ,ε-Epoxy Amide
- Enantioselective Syntheses of Pachastrissamine and Jaspine A via Hydroxylactonization of a Chiral Epoxy Ester
- P-87 Enantioselective Total Synthesis and Stereochemical Revision of Communiols E and F
- Synthesis of (-)-Isishippuric Acid A, a 4,5-Secoquadranoid from a Gorgonian Coral
- Enantioselective Synthesis of Aspergillide B
- Syntheses of (±)-Methyl 6'α-Demethyl-6'α-cyanoabscisate and (±)-Methyl 6'α-Demethyl-6'α-methoxycarbonylabscisate
- A simple, rapid method for gizzerosine analysis in fish meal by paper electrophoresis
- Concise Synthesis of the Anti-HIV Nucleoside EFdA
- Stereoselective Synthesis of a Protected Form of (6R,7E,9S,10R,12Z)-6,9,10-Trihydroxy-7,12-hexadecadienoic Acid