S. Yamauchi

发表

Peptide sequence-dependent gene expression of PEGylated peptide/DNA complexes.

Mikiko Ueno, S. Yamauchi, Daiki Kumekawa, 2019, Molecular pharmaceutics.

Germination Stimulant Activity of Isothiocyanates on Phelipanche spp.

K. Yoneyama, K. Yoneyama, Xiaonan Xie, 2022, Plants.

Synthesis of Amino Tetrahydrofuran Lignan via an N,O-Heterocyclic Compound as an Intermediate

S. Yamauchi, F. Ishibashi, H. Hirao, 2007, Bioscience, biotechnology, and biochemistry.

Effect of Benzylic Oxygen on the Cytotoxic Activity for Colon 26 Cell Line of Phenolic Lignans

S. Yamauchi, T. Sugahara, T. Kishida, 2006, Bioscience, biotechnology, and biochemistry.

Effect of polyphenols on oxymyoglobin oxidation: prooxidant activity of polyphenols in vitro and inhibition by amino acids.

S. Yamauchi, A. Masuda, Yukari Miura, 2013, Journal of agricultural and food chemistry.

Antioxidation reaction mechanism studies of phenolic lignans, identification of antioxidation products of secoisolariciresinol from lipid oxidation

S. Yamauchi, T. Masuda, Y. Sone, 2010 .

Synthesis and Antioxidant Activity of Oxygenated Furofuran Lignans

S. Yamauchi, T. Masuda, Tomoko Ina, 2004, Bioscience, biotechnology, and biochemistry.

Syntheses and Phytotoxicity of All Stereoisomers of 6-(2-Hydroxy-6-phenylhex-1-yl)-5,6-dihydro-2H-pyran-2-one and Determination of Effect of α,β-Unsaturated Carbonyl Structure and Hydroxy Group Bonding to Chiral Carbon.

S. Yamauchi, H. Nishiwaki, Ryo Ochi, 2019, Journal of agricultural and food chemistry.

(-)-Secoisolariciresinol attenuates high-fat diet-induced obesity in C57BL/6 mice.

S. Yamauchi, T. Sugahara, K. Nishi, 2012, Food & function.

Effects of an equol-producing bacterium isolated from human faeces on isoflavone and lignan metabolism in mice.

S. Yamauchi, T. Sugahara, H. Nakagawa, 2016, Journal of the science of food and agriculture.

Effect of the structure of dietary epoxylignan on its cytotoxic activity: relationship between the structure and the activity of 7,7′-epoxylignan and the introduction of apoptosis by caspase 3/7

S. Yamauchi, T. Sugahara, K. Nishi, 2016, Bioscience, biotechnology, and biochemistry.

Immunostimulation Effect of Jellyfish Collagen

S. Yamauchi, T. Sugahara, M. Doi, 2006, Bioscience, biotechnology, and biochemistry.

Hydroxyl carlactone derivatives are predominant strigolactones in Arabidopsis

C. Beveridge, P. Brewer, Mikihisa Umehara, 2020, bioRxiv.

Evaluation of plant growth regulatory activity of furofuran lignan bearing a 7,9':7',9-diepoxy structure using optically pure (+)- and (-)-enantiomers.

H. Ichikawa, S. Yamauchi, Y. Shuto, 2015, Journal of agricultural and food chemistry.

Structure-plant growth inhibitory activity relationship of lariciresinol.

S. Yamauchi, Y. Shuto, H. Nishiwaki, 2013, Journal of agricultural and food chemistry.

Antifungal Activity of Tetra-Substituted Tetrahydrofuran Lignan, (−)-Virgatusin, and Its Structure-Activity Relationship

S. Yamauchi, T. Sugahara, T. Kishida, 2007, Bioscience, biotechnology, and biochemistry.

Synthesis of imidacloprid derivatives with a chiral alkylated imidazolidine ring and evaluation of their insecticidal activity and affinity to the nicotinic acetylcholine receptor.

M. Akamatsu, Hikaru Nagaoka, S. Yamauchi, 2012, Bioorganic & medicinal chemistry.

Stereoselectivity in the Michael Addition Reaction of Dialkylcuprates to the 2-Cyclohexenones with C-4 Ester Substituents.

S. Yamauchi, M. Kadoya, M. Kitagawa, 1998, Bioscience, biotechnology, and biochemistry.

Plant Growth Suppressive Activity of (R)-3-(7'-Aryl-9'-hydroxyprop-8'-yl)coumarin, Structural Isomer of Z-2-Hydroxybenzylidene-γ-butyrolactone-type Lignan.

K. Yoneyama, S. Yamauchi, H. Nishiwaki, 2022, Journal of agricultural and food chemistry.

Stereoselective Synthesis of (2R, 3S)-2-Benzyl-2-hydroxy-3- (3,4-methylenedioxybenzyl)-γ-butyrolactone from L-(+)-Arabinose.

S. Yamauchi, Y. Kinoshita, Y. Kinoshita, 1998, Bioscience, biotechnology, and biochemistry.

Syntheses of cytotoxic novel arctigenin derivatives bearing halogen and alkyl groups on aromatic rings.

S. Yamauchi, T. Sugahara, K. Nishi, 2017, Bioorganic & medicinal chemistry letters.

Reduction of alkyl (2-oxocyclohexyl)acetates by baker's yeast.

M. Motoki, S. Yamauchi, Y. Funabiki, 1998, Bioscience, biotechnology, and biochemistry.

Stereocontrolled syntheses of (-)- and (+)-γ-diisoeugenol along with optically active eight stereoisomers of 7,8'-epoxy-8,7'-neolignan.

S. Yamauchi, H. Nishiwaki, Tatsuaki Takubo, 2021, Organic & biomolecular chemistry.

Transformation of ketones and aldehydes to gem-dihalides via hydrazones using copper(II) halides

S. Yamauchi, T. Fujiwara, T. Takeda, 1997 .

Syntheses of all the stereoisomers of butanol type 1,7-seco-2,7′-cyclolignane

S. Yamauchi, H. Nishiwaki, T. Wukirsari, 2014, Bioscience, biotechnology, and biochemistry.

Syntheses of Secocyclolignanes and Comparative Antioxidative Activity between Secocyclolignane and the Dibenzyl Type of Lignan

S. Yamauchi, T. Masuda, M. Morita, 2011, Bioscience, biotechnology, and biochemistry.

First Diastereoselective Construction of Butane-Type and Butyrolactone-Type Secocyclolignane Structures

S. Yamauchi, M. Morita, 2009, Bioscience, biotechnology, and biochemistry.

First Stereoselective Synthesis of (+)-Magnostellin C, a Tetrahydrofuran Type of Lignan Bearing a Chiral Secondary Benzyl Alcohol

S. Yamauchi, Y. Kinoshita, Y. Kinoshita, 2001, Bioscience, biotechnology, and biochemistry.

Stereoselective Synthesis of Optically Active Methylene Lactone, Key Intermediate for the Synthesis of 1,2-Oxidized Furofuran Lignan, from L-Glutamic Acid.

S. Yamauchi, N. Yamamoto, Y. Kinoshita, 1999, Bioscience, biotechnology, and biochemistry.

Stereoselective Synthesis of (2S,3S)-2-Benzyl-2-hydroxy-3- (3,4-methylenedioxybenzyl)-γ-butyrolactone from L-(+)-Arabinose via a Carissanol-type of Lignan.

S. Yamauchi, Y. Kinoshita, 1998, Bioscience, biotechnology, and biochemistry.

Syntheses of (+)- and (−)-Dihydropinidine and (+)- and (−)-Epidihydropinidine by Using Yeast Reduction of Methyl (2-oxocyclohexyl)acetate

S. Yamauchi, Y. Hirai, Y. Kinoshita, 2004, Bioscience, biotechnology, and biochemistry.

Design of 92 New 9-Norlignan Derivatives and Their Effect on Cell Viabilities of Cancer and Insect Cells.

S. Yamauchi, T. Sugahara, K. Nishi, 2019, Journal of agricultural and food chemistry.

Effect of the Benzylic Structure of Lignan on Antioxidant Activity

S. Yamauchi, T. Sugahara, T. Masuda, 2007, Bioscience, biotechnology, and biochemistry.

Cytotoxic activity of butane type of 1,7-seco-2,7'-cyclolignanes and apoptosis induction by Caspase 9 and 3.

S. Yamauchi, T. Sugahara, K. Nishi, 2014, Bioorganic & medicinal chemistry letters.

First Stereoselective Synthesis of meso-Secoisolariciresinol and Comparison of Its Biological Activity with (+) and (−)-Secoisolariciresinol

S. Yamauchi, T. Sugahara, T. Kishida, 2007, Bioscience, biotechnology, and biochemistry.

Structure-Antifungal Activity Relationship of Fluorinated Dihydroguaiaretic Acid Derivatives and Preventive Activity against Alternaria alternata Japanese Pear Pathotype.

S. Yamauchi, Koichi Akiyama, H. Nishiwaki, 2017, Journal of agricultural and food chemistry.

Synthesis of all stereoisomers of 3,3'-dimethoxy-7,7'-epoxylignane-4,4'-diol and their plant growth inhibitory activity.

S. Yamauchi, Y. Shuto, H. Nishiwaki, 2014, Journal of agricultural and food chemistry.

Syntheses of natural 1,3-polyol/α-pyrone and its all stereoisomers to estimate antifungal activities against plant pathogenic fungi.

S. Yamauchi, Koichi Akiyama, H. Nishiwaki, 2015, Bioorganic & Medicinal Chemistry Letters.

Stereoselective syntheses of cryptocarya diacetate and all its stereoisomers in optically pure forms

S. Yamauchi, H. Nishiwaki, Hiroki Nishimura, 2015, Bioscience, biotechnology, and biochemistry.

Total Syntheses of (−)- and (+)-Boronolide and Their Plant Growth-Inhibitory Activity

S. Yamauchi, Y. Shuto, H. Nishiwaki, 2012, Bioscience, biotechnology, and biochemistry.

Antifungal Activity of Morinol B Derivatives of Tetrahydropyran Sesquilignan

S. Yamauchi, T. Sugahara, K. Masuda, 2010, Bioscience, biotechnology, and biochemistry.

Syntheses of All Stereoisomers of Goniodiol from Yeast-Reduction Products and Their Antimicrobiological Activity

S. Yamauchi, T. Sugahara, T. Kishida, 2008, Bioscience, biotechnology, and biochemistry.

Synthesis of (R)-6,7-dihydro-5-HETE lactone and (S)-6,7-dihydro-5-HETE lactone by using novel yeast reduction as a key reaction

S. Yamauchi, Y. Kinoshita, M. Ganaha, 2002 .

Revised stereochemistry of ficifolidione and its biological activities against insects and cells.

H. Iwamoto, S. Yamauchi, T. Sugahara, 2015, Journal of natural products.

Synthesis of an Optically Pure Synthetic Intermediate of Aloperine from a Yeast-Reductive Product

S. Yamauchi, Yasushi Omi, 2005, Bioscience, biotechnology and biochemistry.

Improved Stereoselective Synthesis of Optically Active Methylene Lactone, Key Intermediate for the Synthesis of 1,2-Oxidized Furofuran Lignan, by Direct α-Methylenation to Butanolide

S. Yamauchi, Y. Kinoshita, N. Yamamoto, 2000, Bioscience, biotechnology, and biochemistry.

Stereoselective Syntheses of (-)-Podorhizol Lignan and its Derivatives: erythro and threo Preferential Aldol Condensation of Potassium Enolate from γ-Butyrolactone with Alkoxybenzaldehyde.

S. Yamauchi, Y. Kinoshita, M. Machi, 1999, Bioscience, biotechnology, and biochemistry.

Evaluation of the highly sensitive chemiluminescent enzyme immunoassay “Lumipulse HBsAg‐HQ” for hepatitis B virus screening

S. Yamauchi, Hiroko Tsukamoto, I. Maeda, 2018, Journal of clinical laboratory analysis.

Oxidation of Hydrazones with Copper(II) Bromide - Lithium t-Butoxide. A Convenient Method for the Transformation of Ketones and Aldehydes to gem-Dibromides

A. Nakamura, S. Yamauchi, T. Fujiwara, 1996 .

Immunomodulatory Effect of (−)-Matairesinol in Vivo and ex Vivo

S. Yamauchi, T. Sugahara, K. Nishi, 2011, Bioscience, biotechnology, and biochemistry.

Mode of Action of the Immunostimulatory Effect of Collagen from Jellyfish

S. Yamauchi, T. Sugahara, M. Doi, 2008, Bioscience, biotechnology, and biochemistry.

The Effect of Secoisolariciresinol on 3T3-L1 Adipocytes and the Relationship between Molecular Structure and Activity

S. Yamauchi, T. Sugahara, T. Kishida, 2009, Bioscience, biotechnology and biochemistry.

Enantioselective syntheses of both enantiomers of 9'-dehydroxyimperanene and 7,8-dihydro-9'-dehydroxyimperanene and the comparison of biological activity between 9-norlignans and dihydroguaiaretic acids.

S. Yamauchi, T. Sugahara, K. Nishi, 2016, Bioorganic & medicinal chemistry letters.

Cytotoxic activity of dietary lignan and its derivatives: structure-cytotoxic activity relationship of dihydroguaiaretic acid.

S. Yamauchi, T. Sugahara, K. Nishi, 2014, Journal of agricultural and food chemistry.

The Structure-Activity Relationships of Flaxseed Lignan, Secoisolariciresinol

S. Yamauchi, T. Sugahara, Y. Kakinuma, 2008 .

Structure-plant phytotoxic activity relationship of 7,7'-epoxylignanes, (+)- and (-)-verrucosin: simplification on the aromatic ring substituents.

S. Yamauchi, Y. Shuto, H. Nishiwaki, 2014, Bioorganic & Medicinal Chemistry Letters.

First discovery of insecticidal activity of 9,9'-epoxylignane and dihydroguaiaretic acid against houseflies and the structure-activity relationship.

S. Yamauchi, Y. Shuto, H. Nishiwaki, 2013, Journal of agricultural and food chemistry.

Stereoselective syntheses of all stereoisomers of lariciresinol and their plant growth inhibitory activities.

S. Yamauchi, Y. Shuto, H. Nishiwaki, 2011, Journal of agricultural and food chemistry.

Disruption of Ion Homeostasis by Verrucosin and a Related Compound

S. Yamauchi, T. Sugahara, Y. Kakinuma, 2011, Bioscience, biotechnology, and biochemistry.

First enantioselective synthesis of (-)- and (+)-virgatusin, tetra-substituted tetrahydrofuran lignan.

S. Yamauchi, T. Sugahara, T. Kishida, 2005, Organic & biomolecular chemistry.

Acute larvicidal activity against mosquitoes and oxygen consumption inhibitory activity of dihydroguaiaretic acid derivatives.

S. Yamauchi, T. Sugahara, K. Nishi, 2015, Journal of agricultural and food chemistry.

Feeding habits of epilachna yasutomii(coleoptera: Coccinellidae) in aomori prefecture, with special reference to temporal invasion of potato fields

S. Yamauchi, 1994 .

Effect of substituents at phenyl group of 7,7'-dioxo-9,9'-epoxylignane on antifungal activity.

S. Yamauchi, T. Sugahara, T. Kishida, 2012, Bioorganic & medicinal chemistry letters.

Effect of benzylic oxygen on the antioxidant activity of phenolic lignans.

S. Yamauchi, T. Masuda, Y. Hayashi, 2005, Journal of natural products.

Syntheses of all eight stereoisomers of conidendrin

S. Yamauchi, H. Nishiwaki, Hinako Shirakata, 2020, Bioscience, biotechnology, and biochemistry.

Synthesis and Insecticidal Activity of Sesquilignan Analogs with 2-Alkyl-6-methoxy-3-(3,4-methylenedioxyphenyl)-1,4-benzodioxanyl Group

S. Yamauchi, E. Taniguchi, 1992 .

Syntheses of 2-Substituted 6/7-Methoxy-l,4-benzodioxan-7/6-carbaldehydes.

S. Yamauchi, T. Ohnishi, E. Taniguchi, 1992, Bioscience, biotechnology, and biochemistry.

Influence on Insecticidal Activity of the 3-(3, 4-Methylenedioxyphenyl) Group in the 1, 4-Benzodioxanyl Moiety of Haedoxan

S. Yamauchi, E. Taniguchi, 1992 .

Synthesis and Insecticidal Activity of Haedoxan Analogs. Part IV. Effect on Insecticidal Activity of Substituents at the 1,4-Benzodioxanyl Moiety of Haedoxan.

S. Yamauchi, E. Taniguchi, S. Nagata, 1992 .

Presence of influenza virus-reactive glycophorins other than glycophorin A in human erythrocyte membranes.

S. Yamauchi, T. Endo, K. Ohyama, 1991, Biochemical and Biophysical Research Communications - BBRC.

Radical and Superoxide Scavenging Activities of Matairesinol and Oxidized Matairesinol

S. Yamauchi, T. Sugahara, T. Masuda, 2006, Bioscience, biotechnology, and biochemistry.

Synthesis and Antioxidant Activity of Olivil-Type Lignans

S. Yamauchi, T. Masuda, Y. Hayashi, 2005, Bioscience, biotechnology, and biochemistry.

First highly stereoselective synthesis of (+)-dihydrosesamin, a trisubstituted tetrahydrofuran-type of lignan, by using highly erythro-selective aldol condensation

S. Yamauchi, Y. Kinoshita, Teruhisa Tanaka, 2001 .

First Highly Stereoselective Synthesis of (+)-Dihydrosesamin, a Trisubstituted Tetrahydrofuran-Type of Lignan, by Using Highly erythro-Selective Aldol Condensation.

S. Yamauchi, Y. Kinoshita, Teruhisa Tanaka, 2002 .

Synthesis of (+)-(1S, 2S, 5R, 6S)-1-Hydroxysamin from L-(+)-Arabinose

S. Yamauchi, Y. Kinoshita, 1997 .

Synthesis of 1,2-Oxygenated 6-arylfurofuran Lignan: Stereoselective Synthesis of (1S,2S,5R,6S)-1-hydroxysamin

S. Yamauchi, Y. Kinoshita, S. Bando, 2002, Bioscience, biotechnology and biochemistry.

Stereoselective Model Synthesis of the Optically Active Olivil Type of Lignan from D-Xylose

S. Yamauchi, Y. Kinoshita, 2000, Bioscience, biotechnology and biochemistry.

Synthesis of 1 , 2-Oxygenated 6-arylfurofuran Lignan : Stereoselective Synthesis of ( 1 S , 2 S , 5 R , 6 S )-1-hydroxysamin

S. Yamauchi, Y. Kinoshita, S. Bando, 2003 .

Synthesis of cis-Lactone Lignan, cis-(2S,3R)-Parabenzlactone, from L-Arabinose

S. Yamauchi, Y. Kinoshita, 2001, Bioscience, biotechnology, and biochemistry.

Synthesis of Optically Active Olivil Type of Lignan from L-Arabinose Using threo-Selective Aldol Condensation as a Key Reaction

S. Yamauchi, Y. Kinoshita, 2000, Bioscience, biotechnology, and biochemistry.

Use of the Benzyl Mesylate for the Synthesis of Tetrahydrofuran Lignan: Syntheses of 7,8-trans, 7′,8′-trans, 7,7′-cis, and 8,8′-cis-Virgatusin Stereoisomers

S. Yamauchi, T. Sugahara, T. Kishida, 2007, Bioscience, biotechnology, and biochemistry.

Synthesis of (+)-Aptosimon, a 4-Oxofurofuran Lignan, by erythro Selective Aldol Condensation and Stereoconvergent Cyclization as the Key Reactions

S. Yamauchi, Munetoshi Yamaguchi, 2003, Bioscience, biotechnology, and biochemistry.

Syntheses of 6-(2-hydroxy-6-phenylhexyl)-5,6-dihydro-2H-pyran-2-one derivatives and their cytotoxicities

S. Yamauchi, T. Sugahara, K. Nishi, 2022, Phytochemistry Letters.

Structure-Antibacterial Activity Relationship for 9-O,9′-O-Demethyl (+)-virgatusin

S. Yamauchi, T. Sugahara, T. Kishida, 2008, Bioscience, biotechnology, and biochemistry.

Antibacterial Activity of a Virgatusin-Related Compound

S. Yamauchi, T. Sugahara, T. Kishida, 2007, Bioscience, biotechnology, and biochemistry.

Structure-cytotoxic activity relationship of sesquilignan, morinol A.

S. Yamauchi, T. Sugahara, K. Nishi, 2013, Bioorganic & medicinal chemistry letters.

Improved Syntheses of Morinol C and D by Employing Mizoroki-Heck Reaction and Their Cytotoxic and Antimicrobial Activities

S. Yamauchi, T. Sugahara, Koichi Akiyama, 2010, Bioscience, biotechnology, and biochemistry.

Discovery of stereospecific cytotoxicity of (8R,8'R)-trans-arctigenin against insect cells and structure-activity relationship on aromatic ring.

S. Yamauchi, T. Sugahara, K. Nishi, 2020, Bioorganic & Medicinal Chemistry Letters.

Antimicrobial Activity of Stereoisomers of Butane-Type Lignans

S. Yamauchi, T. Sugahara, K. Masuda, 2009, Bioscience, biotechnology, and biochemistry.

Effects of Substituents on the Aromatic Ring of Lignano-9,9'-lactone on Plant Growth Inhibitory Activity.

S. Yamauchi, H. Nishiwaki, Asuka Nishimoto, 2018, Journal of agricultural and food chemistry.

Quantitative structure-activity relationship analysis of antifungal (+)-dihydroguaiaretic acid using 7-phenyl derivatives.

S. Yamauchi, T. Sugahara, T. Kishida, 2013, Journal of agricultural and food chemistry.

Larvicidal Activity of (−)-Dihydroguaiaretic Acid Derivatives against Culex pipiens

M. Akamatsu, S. Yamauchi, Y. Shuto, 2011, Bioscience, biotechnology, and biochemistry.

IgE-Suppressive Activity of (−)-Matairesinol and Its Structure-Activity Relationship

S. Yamauchi, T. Sugahara, T. Kishida, 2010, Bioscience, biotechnology, and biochemistry.

Antimicrobial Activity of Stereoisomers of Morinols A and B, Tetrahydropyran Sesquineolignans

S. Yamauchi, T. Sugahara, T. Kishida, 2009, Bioscience, biotechnology, and biochemistry.

Stereoselective Synthesis of the Optically Active Samin Type of Lignan from L-Glutamic Acid

S. Yamauchi, Y. Kinoshita, N. Yamamoto, 2000, Bioscience, biotechnology, and biochemistry.

Effects of an equol-producing bacterium isolated from human faeces on isoflavone and lignan metabolism in mice.

S. Yamauchi, T. Sugahara, H. Nakagawa, 2016, Journal of the science of food and agriculture.

Antimicrobiological Activity of Lignan: Effect of Benzylic Oxygen and Stereochemistry of 2,3-Dibenzyl-4-butanolide and 3,4-Dibenzyltetrahydrofuran Lignans on Activity

S. Yamauchi, T. Sugahara, T. Kishida, 2007, Bioscience, biotechnology, and biochemistry.

Syntheses of Tetrahydropyran Type 8,7'-Neolignans Using a Ring-Expansion Reaction and Tetrahydrofuran Type 8,7'-Neolignans to Discover a Novel Phytotoxic Neolignan.

S. Yamauchi, H. Nishiwaki, Miyo Tanaka, 2023, Journal of agricultural and food chemistry.

Cytotoxicity against HL60 Cells of Ficifolidione Derivatives with Methyl, n-Pentyl, and n-Heptyl Groups

S. Yamauchi, T. Sugahara, K. Nishi, 2019, Molecules.

Enantioselective synthesis of the tetrahydrofuran lignans (-)- and (+)-magnolone.

S. Yamauchi, Tomofumi Nakato, 2007, Journal of natural products.