Synthesis of (S)-β-Blockers from (S)-5-Hydroxymethyl-3-tert butyl-2-oxazolidinone or (S)-5-Hydroxymethyl-3-isopropyl-2-oxazolidinone
スポンサーリンク
概要
著者
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Watanabe Kiyoshi
Biochemical Research Laboratories Kanegafuchi Chemical Industry Co. Ltd.
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Ohashi Takehisa
Biochemical Research Laboratories Kanegafuchi Chemical Industry Co. Ltd.
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KAN Kazunori
Biochemical Research Laboratories, Kanegafuchi Chemical Industry Co., Ltd.
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MIYAMA Akimasa
Biochemical Research Laboratories, Kanegafuchi Chemical Industry Co., Ltd.
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Hamaguchi Shigeki
Biochemical Research Laboratories Kanegafuchi Chemical Industry Co. Ltd.
関連論文
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- Comparison of Human Lymphotoxin Gene Expression in CHO Cells Directed by Genomic DNA or cDNA Sequences(Biological Chemistry)
- High-yield Production of Optically Active 1,2-Diols from the Corresponding Racemates by Microbial Stereoinversion(Microbiology & Fermentation Industry)
- Asymmetric Hydrolysis of (dl)-1-Acyloxy-2-halo-1-phenylethanes with Lipases(Organic Chemistry)
- Lipase-catalyzed Stereoselective Hydrolysis of 2-Acyl and 1-p-Tolylsulfonyl Substituted Propanediol and Butanediol
- Stereochemical Inversion of (R)-5-Hydroxymethyl-3-tert-butyl-2-oxazolidinone or (R)-5-Hydroxymethyl-3-isopropyl-2-oxazolidinone to the Corresponding (S)-Isomer
- Heat-induced Gelation of a Mixture of Myosin B and Soybean Protein
- A New Method for 5-(4-Hydroxyphenyl)hydantoin Synthesis
- Microbial Production of (R)-3-Halolactic Acid from(±)-3-Halo-1,2-Propanediol
- Stereospecific Hydrolysis of 2-Oxazolidinone Esters and Separation of Products with an Immobilized Lipase Column
- Production of D-β-Hydroxycarboxylic Acids from the Corresponding Carboxylic Acids by a Mutant of Candida rugosa : Studies of β-Hydroxycarboxylic Acids (V)
- Production of β-Hydroxypropionic Acid from Propionic Acid by a Candida rugosa Mutant Unable to Assimilate Propionic Acid : Studies on β-Hydroxycarboxylic Acids (IV)
- Production of d-β-Hydroxyisobutyric Acid from Isobutyric Acid by Candida rugosa and Its Mutant : Studies on β-Hydroxycarboxylic Acids (III)
- Produciton of β-Hydroxycarboxylic Acids from Aliphatic Carboxylic Acids by Microorganisms : Studies on β-Hydroxycarboxylic Acids (II)
- Stereoselective Conversion of Isobutyric Acid to β-Hydroxyisobutyric Acid by Microoganisms : Studies on β-Hydroxycarboxylic Acids (I)
- Enzymatic Resolution of 2-Oxazolidinone Estersf
- The Pharmacokinetic Pattern of Glycosylated Human Recombinant Lymphotoxin (LT) in Rats after Intravenous Administration
- Lipase-catalyzed Stereoselective Hydrolysis of 2-Acyloxy-3-chloropropyl p-toluenesulfonate
- Asymmetric Hydrolysis of (R, S)-5-Acetoxymethyl-3-terr-butyl-oxazolidin-2-one with Enzymes and Microorganisms
- Effect of .ALPHA.-(3,5-di-tert-butyl-4-hydroxybenzylidene)-.GAMMA.-butyrolactone (KME-4), a new anti-inflammatory drug, on the established adjuvant arthritis in rats.
- Pharmacological properties of a new anti-inflammatory compound, .ALPHA.-(3,5-di-tert-butyl-4-hydroxybenzylidene)-.GAMMA.-butyrolactone (KME-4), and its inhibitory effects on prostaglandin synthetase and 5-lipoxygenase.
- Inhibition of polymorphonuclear leukocyte 5-lipoxygenase and platelet cyclooxygenase by .ALPHA.-(3,5-di-tert-butyl-4-hydroxybenzylidene)-.GAMMA.-butyrolactone (KME-4), a new anti-inflammatory drug.
- Synthesis of (S)-β-Blockers from (S)-5-Hydroxymethyl-3-tert butyl-2-oxazolidinone or (S)-5-Hydroxymethyl-3-isopropyl-2-oxazolidinone