UB Paderborn / Katalog / Suche / in CDI

2013 Transducers & Eurosensors XXVII: The 17th International Conference on Solid-State Sensors, Actuators and Microsystems (TRANSDUCERS & EUROSENSORS XXVII), 2013, p.784-787

2013

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Synthetic Studies on Clerodane Diterpenoids-A Case of the Stereocontrols in Natural Products Synthesis

Journal of Synthetic Organic Chemistry, Japan, 1993/12/01, Vol.51(12), pp.1164-1177

TOKOROYAMA, Takashi

1993

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Studies on the Preparation of Bioactive Lignans by Oxidative Coupling Reaction. I. Preparation and Lipid Peroxidation Inhibitory Effect of Benzofuran Lignans Related to Schizotenuins

Chemical and Pharmaceutical Bulletin, 1994/12/15, Vol.42(12), pp.2500-2505

1994

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Studies on the preparation of bioactive lignans by oxidative coupling reaction. IV: Oxidative coupling reaction of methyl (E)-3-(3,4-dihydroxy-2-methoxyphenyl)propenoate and lipid peroxidation inhibory effects of the produced lignans

Chemical & pharmaceutical bulletin, 1995, Vol.43 (1), p.84-90

1995

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The biosynthesis of sclerin

Journal of the Chemical Society. C. Organic, 1971, p.2703

1971

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Studies on the preparation of bioactive lignans by oxidative coupling reaction. III: Synthesis of polyphenolic benzofuran and coumestan derivatives by oxidation coupling reaction of methyl (E)-3-(4-hydroxy-2-methoxyphenyl) propenoate and their inhibitory effect on lipid peroxidation

Chemical & pharmaceutical bulletin, 1994, Vol.42 (12), p.2536-2545

1994

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Further phenolic components from Alnus japonica Steud

Journal of the Chemical Society. Chemical communications, 1975 (9), p.316

1975

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ChemInform Abstract: Synthetic Studies on Clerodane Diterpenoids. A Case of the Stereocontrols in Natural Products Synthesis

ChemInform, 1994-05, Vol.25 (21), p.no-no

TOKOROYAMA, T.

1994

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Studies on the Preparation of Bioactive Lignans by Oxidative Coupling Reaction. V. Oxidative Coupling Reaction of Methyl (E)-3-(2-Hydroxyphenyl)propenoate Derivatives and Lipid Peroxidation Inhibitory Effects of the Produced Lignans

Chemical and Pharmaceutical Bulletin, 1995/06/15, Vol.43(6), pp.935-940

1995

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Influence of Defects in Graphene-Like Network of Diamond-Like Carbon on Silica Scale Adhesion

The ta-C Hardness Effect on Wear Properties Under MoDTC Contained Boundary Lubrication

SAT0059 Chronic Kidney Disease in Patients with Rheumatoid Arthritis: Clinical Findings from a Longitudinal Study Over 5 Years in a Single Tertiary Hospital

The 1 μm wear particles entrainment in situ observation via fluorescent staining silica particles by silane coupling with Rhodamine B

Effect of nitrogen atoms desorption on the friction of the CNx coating against Si3N4 ball in nitrogen gas

Portulene Acetal, a Novel Minor Constituent of Portulaca grandiflora with Significance for the Biosynthesis of Portulal

The effect of ultraviolet light irradiation on tribological properties of hydrogenated DLC

Diastereofacial Selection in Ring-Closure Reactions and Folding-Strain Stereocontrol

Studies on the Preparation of Bioactive Lignans by Oxidative Coupling Reaction. IV. Oxidative Coupling Reaction of Methyl (E)-3-(3, 4-Dihydroxy-2-methoxyphenyl)propenoate and Lipid Peroxidation Inhibitory Effects of the Produced Lignans

Studies on the Preparation of Bioactive Lignans by Oxidative Coupling Reaction. II. Oxidative Coupling Reaction of Methyl (E)-3-(4, 5-Dihydroxy-2-methoxyphenyl)propenoate and Lipid Peroxidation Inhibitory Effects of the Produced Lignans

Studies on the Preparation of Bioactive Lignans by Oxidative Coupling Reaction. VI. Oxidation of Methyl (E)-3-(4, 5-Dihydroxy-2-methoxyphenyl)-2-butenoate and Lipid Peroxidation-Inhibitory Effects of the Produced Caffeoquinone

Doubly Diastereocontrolled Cyclization Based on Intramolecular Conjugate Addition Reactions Involving an Allylic Radical and an Anion

Folding Strain Stereocontrol: Diastereoselectivity in Ring-Closure Reaction

Synthetic Studies on Limonoids

Folding strain stereocontrol in cyclohexane ring formation by means of an intramolecular ester enolate alkylation reaction

Effect of surface roughness and transfer layer of mating ceramic parts for ultra low friction phenomena in sliding between CNx and ceramics

Direct observation of damage accumulation process inside silicon under mechanical fatigue loading

Synthetic Studies on Clerodane Diterpenoids-A Case of the Stereocontrols in Natural Products Synthesis

Studies on the Preparation of Bioactive Lignans by Oxidative Coupling Reaction. I. Preparation and Lipid Peroxidation Inhibitory Effect of Benzofuran Lignans Related to Schizotenuins

Studies on the preparation of bioactive lignans by oxidative coupling reaction. IV: Oxidative coupling reaction of methyl (E)-3-(3,4-dihydroxy-2-methoxyphenyl)propenoate and lipid peroxidation inhibory effects of the produced lignans

The biosynthesis of sclerin

Studies on the preparation of bioactive lignans by oxidative coupling reaction. III: Synthesis of polyphenolic benzofuran and coumestan derivatives by oxidation coupling reaction of methyl (E)-3-(4-hydroxy-2-methoxyphenyl) propenoate and their inhibitory effect on lipid peroxidation

Further phenolic components from Alnus japonica Steud

ChemInform Abstract: Synthetic Studies on Clerodane Diterpenoids. A Case of the Stereocontrols in Natural Products Synthesis

Studies on the Preparation of Bioactive Lignans by Oxidative Coupling Reaction. V. Oxidative Coupling Reaction of Methyl (E)-3-(2-Hydroxyphenyl)propenoate Derivatives and Lipid Peroxidation Inhibitory Effects of the Produced Lignans

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