Structures and Absolute Configurations of New Lobane Diterpenoids from the Okinawan Soft Coral Sinularia flexibilis
スポンサーリンク
概要
- 論文の詳細を見る
- 1992-01-05
著者
-
Kusumi T
Faculty Of Pharmaceutical Sciences The University Of Tokushima
-
Kusumi Takenori
Department Of Chemistry University Of Tsukuba
-
Hamada Toshiyuki
Department Of Cardiovascular Surgery Kanagawa Cardiovascular And Respiratory Center
-
Hamada Toshiyuki
Department Of Chemistry University Of Tsukuba
-
ISHITSUKA Midori
Department of Chemistry, University of Tsukuba
-
KAKISAWA Hiroshi
Department of Chemistry, University of Tsukuba
-
Kakisawa Hiroshi
Department Of Chemistry University Of Tsukuba
-
Ishitsuka Midori
Department Of Chemistry University Of Tsukuba
関連論文
- Oxidation of Cyclopropane Terpenoids with Ruthenium Tetraoxide
- Chiral Anisotropic Reagents for Determining the Absolute Configuration of Secondary Alcohols and Carboxylic Acids
- Absolute Configurations of Some Hydroxy-fatty Acids Produced by the Insect Genus Laccifer
- The Modified Mosher's Method and the Sulfoximine Method
- A new diterpene dimer from the bark of Chamaecyparis obtusa
- Carbon-13 Spin-Lattice Relaxation Time (T1) for Assignment of Brominated Carbons
- Influence of the Conformation of Methoxy-(2-naphthyl)acetates (2NMA Esters) on Their Chemical Reactions
- Etching Characteristics of Fabricated Grooves on Silicon Solar Cell using Surface Discharge Plasma
- Structures and Absolute Configurations of New Lobane Diterpenoids from the Okinawan Soft Coral Sinularia flexibilis
- Surgical Case of Isolated Pulmonary Takayasu's Arteritis
- One-step Preparation of Gold Nanoparticles Using 4-Acylamidobenzenethiol as a Reductive Stabilizer
- Examination of Maskless Etching Technique Using a Localized Surface Discharge Plasma
- Pa17 ABSOLUTE STEREOCHEMISTRY OF SOME MARINE DITERPENES : CONSIDERATION ON THE VALIDITY OF MOSHER'S RULE
- Acceleration of Tributyltin Hydride Reduction of Phenethyl Iodide and m-Methoxybenzyl Bromide by a Strong Magnetic Field
- 9.4T and 7.05T Magnetic Fields Accelerate a Radical Oxidation Reaction with a Hypervalent (tert-Butylperoxy)iodane
- Synthesis of dl-3-hydroxycuparene by a Claisen rearrangement of allyl aryl ether.
- Acyliminium cyclization of several chiral N-alkenylsuccinimide derivatives.
- A short-step synthesis of 4-hydroxyproline.
- The Acid-Catalyzed Cyclization of 2,3-Dimethyl-2-phenethyl-3-cyclohexen-1-one
- Selective Etching of Silicon Nitride Film on Single Crystalline Silicon Solar Cell Using Intensive Surface Discharge
- Structures of Lignans of Magnolia fargesii
- Preparation of bicyclo[3.3.1]nonane-2,4-dione derivatives.
- A quinone and a phenol from a Myrsinaceae plant.
- Intramolecular (2+2)photocycloaddition of the 3-(3-butenyloxy)-2-cyclohexenone system.
- Effective cleavage of 7-alkoxytricyclo(6.4.0.02,7)dodecan-3-one system.
- Structures of Diterpenoid Tropolones, Salviolone and Miltipolone from the Root of Salvia miltiorrhiza Bunge.
- Synthesis of (.+-.)-hernandulcin by an intramolecular nitrile oxide cycloaddition route from farnesol.
- New synthesis of .GAMMA.-hydroxyglutamic acid.
- Synthesis of Furonaphthoquinones
- Regio- and facial-selective effects of allylic heteroatoms in 1,3-dipolar cycloaddition of a nitrile oxide.
- Preparation of 2-oxabicyclo(2.2.2)oct-5-ene, 1,4-dimethyl-2-oxabicyclo-(2.2.2)oct-5-ene, and 6-oxabicyclo(3.2.1)oct-3-ene.
- The Synthesis of 24-Norfriedel-4-en-3-one
- A convenient synthesis of condensed cyclopentane system. Annelation by intramolecular 1,3-dipolar addition of nitrones.
- Hydrogenolysis of a Quinonoid Oxygen of Alkoxynaphthoquinones
- The configurations of N-methyl- and N-t-butyl-.ALPHA.-methoxycarbonylmethanimine N-oxides.
- Preparation of several 1,5,5,11,11-pentamethyltricyclo-(6.2.1.02,6)undecane derivatives.
- Synthesis of salvilenone, a diterpenoid phenalenone of Salvia miltiorrhiza.