Synthesis of the A-and B-Ring System of Hemibrevetoxin-B
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概要
- 論文の詳細を見る
- 1995-01-05
著者
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Murai Akio
Department Of Chemistry Faculty Of Science Hokkaido University
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FENG Fei
Department of Chemistry, Faculty of Science, Hokkaido University
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Feng Fei
Department Of Chemistry Faculty Of Science Hokkaido University
関連論文
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- Synthesis of the Tetrahydrofuran Ring Part of a Marine Toxin Polycavernoside-A
- PD27 HYDROGEN PEROXIDE ACTS AS AN ENDOGENOUS ELICITOR FOR PHYTOALEXIN PRODUCTION
- Synthesis and Relative Configuration of the Sugar Part of a Marine Toxin Polycavernoside-A
- Synthesis of the Tetrahydropyran Ring Part of a Marine Toxin Polycavernoside-A
- Isomerization of the (Z)-Enyne Unit to the (E)-Enyne Unit. Conversion of Laureatin to (E)-Isolaureatin
- Isolation of an Endogenous Elicitor Induced by Hydrogen Peroxide from Potato
- Hydrogen Peroxide as a Dynamic Trigger for Phytoalexin Production
- Synthesis of the C- and D-Ring System of Hemibrevetoxin-B
- Structure-activity Relationship of Glycinoeclepin A
- Enzymatic Bromo-ether Cyclization of Laurediols with Bromoperoxidase
- Production of Potato Cyst Nematode Hatching Stimulus by Hairy Root Cultures of Tomato(Microbiology & Fermentation Industry)
- SLB5 TOTAL SYNTHESIS OF GLYCINOECLEPIN A
- Synthesis of the A-and B-Ring System of Hemibrevetoxin-B
- Biological activities of rishitin, an antifungal compound isolated from diseased potato tubers, and its derivatives
- The structure and configuration of (+)-glutionosone and (+)-oxyglutinosone.
- Structure of rishitione, a valencane stress metabolite in diseased potato.
- Synthesis of .BETA.- and .ALPHA.-rotunols. Revision of the structure of a stress metabolite "1-keto-.ALPHA.-cyperone".
- Structure of epilubimin, epioxylubimin, and isolubimin, spirovetivane stress metabolites in diseased potato.
- Synthesis of phytuberin.
- Total synthesis of (.+-.)-lubimin and (.+-.)-oxylubimin. II. Transformation of (.+-.)-15-norsolavetivanes into (.+-.)-lubimin, (.+-.)-oxylubimin, and related compounds.
- Photooxygenation of .ALPHA.,.BETA.- and .BETA.,.GAMMA.-unsaturated enamines in 17-(1-formylethyl)etiojervanes.
- Stereochemistry of the C and D rings of C-nor-D-homosteroid. IV. The relative stabilities and NMR spectra of 17-substituted C/D trans- and cis-fused etiojervanes.
- Stereochemistry of the C and D rings of C-nor-D-homesteroids. III. The synthesis of etiojervane analogs of androstan-3.BETA.ol.
- Rishitin. I. The isolation and structure elucidation.
- 12,13-Epoxy-C-nor-D-homosteroids. VI. Reaction of 17-oxygenated 12,13-epoxyetiojervanes with boron trifluoride etherate.
- 12,13-Epoxy-C-nor-D-homosteroids. VIII. Transformation of 12.ALPHA.,13.ALPHA.-epoxyetiojerv-5-ene-3,17-dione 3,3-ethylene acetal into testosterone.
- 12,13-Epoxy-C-nor-D-homosteroids. VII. Reaction of 11-oxygenated 17.ALPHA.-acetyl-12.BETA.,13.BETA.-epoxy-13-epietiojervanes with boron trifluoride etherate and potassium hydroxide.
- Total synthesis of (.+-.)-lubimin and (.+-.)-oxylubimin. I. Synthesis of (.+-.)-15-norsolavetivone and related compounds.
- A general synthetic approach of spirovetivanes. The synthesis of (.+-.)-solavetivone, (.+-.)-hinesol, and related compounds.
- Synthesis of aubergenone, a sesquiterpenoid phytoalexin from diseased eggplants.
- Steric effect in regioselective cyclization of 3,4-epoxy alcohols to oxetanes.
- The configuration of 17-ethyl-3.BETA.-hydroxyetiojerva-5,12,17(20)-trien-11-one and related compounds.
- Synthetic studies of laurencin and related compounds. V. Transformation of cis-2-ethyl-8-formyl-3,4,7,8-dihydro-2H-oxocin-3-one 3-ethylene acetal into (.+-.)-laurencin.
- Intramolecular cyclization of 3,4-epoxy alcohols; oxetane formation.
- Stereochmistry of the C and D rings of C-nor-D-homosteroids. II. Synthesis of etiojervane analogs of pregnan-3.BETA.-ol.
- Lubimin and oxylubimin. The structure elucidation.
- 12,13-Epoxy-C-nor-D-homosteroids. III. The synthesis and stereochemistry of 17-oxygenated 12,13-epoxyetiojervanes.
- 12,13-Epoxy-C-nor-D-homosteroids. I. The synthesis and stereochemistry of 17.ALPHA.-acetyl-12,13-epoxyetiojervanes.
- 12,13-Epoxy-C-nor-D-homosteroids. IV. The reaction of 11-oxygenated 17.ALPHA.-acetyl-12.ALPHA.,13.ALPHA.-epoxyetiojervanes with boron trifluoride etherate.