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Satoshi Yamauchi
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Chemicals & Drugs
Genes & Molecular Sequences
Phenomena
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Network (preview)
21
Sugahara, Takuya
20
Akiyama, Koichi
19
Kishida, Taro
16
Maruyama, Masafumi
10
Kinoshita, Yoshiro
6
Masuda, Toshiya
6
Nakashima, Yuki
6
Nakato, Tomofumi
3
Hayashi, Yoshimasa
3
Kirikihira, Takuya
1
Uno, Hidemitsu
1
Kashiwagi, Takehiro
1
Bando, Shiro
1
Okazaki, Momotoshi
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Geonetwork of Satoshi Yamauchi (preview)
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All Publications
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2009: Kawaguchi Yuya; Yamauchi Satoshi; Masuda Kenta; Nishiwaki Hisashi; Akiyama Koichi; Maruyama Masafumi; Sugahara Takuya; Kishida Taro; Koba Yojiro
Antimicrobial activity of stereoisomers of butane-type lignans.
Bioscience, biotechnology, and biochemistry 2009;73(8):1806-10.
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2009: Yamauchi Satoshi; Kishida Taro; Sugahara Takuya; Yamawaki Manami; Nishimoto Sogo; Shinomiya Yoh-ichi; Yamamoto Toru
Inhibition of the discoloration of yellowtail dark muscle by lignan.
Bioscience, biotechnology, and biochemistry 2009;73(8):1718-21.
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2009: Nakato Tomofumi; Yamauchi Satoshi; Tago Ryosuke; Akiyama Koichi; Maruyama Masafumi; Sugahara Takuya; Kishida Taro; Koba Yojiro
Syntheses and antimicrobial activity of tetrasubstituted tetrahydrofuran lignan stereoisomers.
Bioscience, biotechnology, and biochemistry 2009;73(7):1608-17.
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2009: Tominaga Shiori; Sugahara Takuya; Nishimoto Sogo; Yamawaki Manami; Nakashima Yuki; Kishida Taro; Akiyama Koichi; Maruyama Masafumi; Yamauchi Satoshi
The Effect of Secoisolariciresinol on 3T3-L1 Adipocytes and the Relationship between Molecular Structure and Activity.
Bioscience, biotechnology, and biochemistry 2009;73(1):35-9.
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2009: Akiyama Koichi; Yamauchi Satoshi; Maruyama Masafumi; Sugahara Takuya; Kishida Taro; Koba Yojiro
Antimicrobial activity of stereoisomers of morinols a and B, tetrahydropyran sesquineolignans.
Bioscience, biotechnology, and biochemistry 2009;73(1):129-33.
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2008: Nishimoto Sogo; Goto Yoko; Morishige Hitoshi; Shiraishi Ryusuke; Doi Mikiharu; Akiyama Koichi; Yamauchi Satoshi; Sugahara Takuya
Mode of action of the immunostimulatory effect of collagen from jellyfish.
Bioscience, biotechnology, and biochemistry 2008;72(11):2806-14.
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2008: Yamauchi Satoshi; Masuda Toshiya; Sugahara Takuya; Kawaguchi Yuya; Ohuchi Maya; Someya Tatsushi; Akiyama Jun; Tominaga Shiori; Yamawaki Manami; Kishida Taro; Akiyama Koichi; Maruyama Masafumi
Antioxidant activity of butane type lignans, secoisolariciresinol, dihydroguaiaretic acid, and 7,7'-oxodihydroguaiaretic acid.
Bioscience, biotechnology, and biochemistry 2008;72(11):2981-6.
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2008: Yoshida Takahiro; Yamauchi Satoshi; Tago Ryosuke; Maruyama Masafumi; Akiyama Koichi; Sugahara Takuya; Kishida Taro; Koba Yojiro
Syntheses of all stereoisomers of goniodiol from yeast-reduction products and their antimicrobiological activity.
Bioscience, biotechnology, and biochemistry 2008;72(9):2342-52.
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2008: Tago Ryosuke; Yamauchi Satoshi; Maruyama Masafumi; Akiyama Koichi; Sugahara Takuya; Kishida Taro; Koba Yojiro
Structure-antibacterial activity relationship for 9-O,9'-O-demethyl (+)-virgatusin.
Bioscience, biotechnology, and biochemistry 2008;72(4):1032-7.
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2008: Nakato Tomofumi; Tago Ryosuke; Akiyama Koichi; Maruyama Masafumi; Sugahara Takuya; Kishida Taro; Yamauchi Satoshi
Stereoselective construction of tetra-substituted tetrahydrofuran compounds from benzylic hemiacetal in the presence of H2 and a Pd catalyst: stereoselective synthesis of a stereoisomer of (-)-virgatusin and its antimicrobiological activity.
Bioscience, biotechnology, and biochemistry 2008;72(1):197-203.
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2007: Sugahara Takuya; Yamauchi Satoshi; Kondo Ai; Ohno Fumi; Tominaga Siori; Nakashima Yuki; Kishida Taro; Akiyama Koichi; Maruyama Masafumi
First stereoselective synthesis of meso-secoisolariciresinol and comparison of its biological activity with (+) and (-)-secoisolariciresinol.
Bioscience, biotechnology, and biochemistry 2007;71(12):2962-8.
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2007: Nakato Tomofumi; Yamauchi Satoshi
Enantioselective synthesis of the tetrahydrofuran lignans (-)- and (+)-magnolone.
Journal of natural products 2007;70(10):1588-92.
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2007: Yamauchi Satoshi; Nakato Tomofumi; Tsuchiya Masahiro; Akiyama Koichi; Maruyama Masafumi; Sugahara Takuya; Kishida Taro
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.
Bioscience, biotechnology, and biochemistry 2007;71(9):2248-55.
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2007: Yamauchi Satoshi; Sugahara Takuya; Matsugi Junko; Someya Tatsushi; Masuda Toshiya; Kishida Taro; Akiyama Koichi; Maruyama Masafumi
Effect of the benzylic structure of lignan on antioxidant activity.
Bioscience, biotechnology, and biochemistry 2007;71(9):2283-90.
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2007: Akiyama Koichi; Maruyama Masafumi; Yamauchi Satoshi; Nakashima Yuki; Nakato Tomofumi; Tago Ryosuke; Sugahara Takuya; Kishida Taro; Koba Yojiro
Antimicrobiological activity of lignan: effect of benzylic oxygen and stereochemistry of 2,3-dibenzyl-4-butanolide and 3,4-dibenzyltetrahydrofuran lignans on activity.
Bioscience, biotechnology, and biochemistry 2007;71(7):1745-51.
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2007: Akiyama Koichi; Yamauchi Satoshi; Nakato Tomofumi; Maruyama Masafumi; Sugahara Takuya; Kishida Taro
Antifungal activity of tetra-substituted tetrahydrofuran lignan, (-)-virgatusin, and its structure-activity relationship.
Bioscience, biotechnology, and biochemistry 2007;71(4):1028-35.
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2007: Yamauchi Satoshi; Sugahara Takuya; Akiyama Koichi; Maruyama Masafumi; Kishida Taro
Determination of the stereochemistry of the tetrahydropyran sesquineolignans morinols A and B.
Journal of natural products 2007;70(4):549-56.
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2007: Hirao Haruna; Yamauchi Satoshi; Ishibashi Fumito;
Synthesis of amino tetrahydrofuran lignan via an N,O-heterocyclic compound as an intermediate.
Bioscience, biotechnology, and biochemistry 2007;71(3):741-5.
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2007: Maruyama Masafumi; Yamauchi Satoshi; Akiyama Koichi; Sugahara Takuya; Kishida Taro; Koba Yojiro
Antibacterial activity of a virgatusin-related compound.
Bioscience, biotechnology, and biochemistry 2007;71(3):677-80.
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2006: Yamauchi Satoshi; Sugahara Takuya; Nakashima Yuki; Abe Koki; Hayashi Yoshimasa; Akiyama Koichi; Kishida Taro; Maruyama Masafumi
Effect of benzylic oxygen on the cytotoxic activity for colon 26 cell line of phenolic lignans.
Bioscience, biotechnology, and biochemistry 2006;70(12):2942-7.
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2006: Sugahara Takuya; Ueno Masashi; Goto Yoko; Shiraishi Ryusuke; Doi Mikiharu; Akiyama Koichi; Yamauchi Satoshi
Immunostimulation effect of jellyfish collagen.
Bioscience, biotechnology, and biochemistry 2006;70(9):2131-7.
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2006: Yamauchi Satoshi; Sugahara Takuya; Nakashima Yuki; Okada Akihiro; Akiyama Koichi; Kishida Taro; Maruyama Masashi; Masuda Toshiya
Radical and superoxide scavenging activities of matairesinol and oxidized matairesinol.
Bioscience, biotechnology, and biochemistry 2006;70(8):1934-40.
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2006: Mori Shunji; Iwamoto Shoko; Yamauchi Satoshi
Synthesis of a glandular secretion of the civet cat, (2S,6S)-(6-methyltetrahydropyran-2-yl)acetic acid and its enantiomer, by using the yeast-reduction product and recovered substrate from yeast reduction.
Bioscience, biotechnology, and biochemistry 2006;70(3):712-7.
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2005: Yamauchi Satoshi; Hayashi Yoshimasa; Nakashima Yuki; Kirikihira Takuya; Yamada Kazuki; Masuda Toshiya
Effect of benzylic oxygen on the antioxidant activity of phenolic lignans.
Journal of natural products 2005;68(10):1459-70.
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2005: Yamauchi Satoshi; Omi Yasushi
Synthesis of an optically pure synthetic intermediate of aloperine from a yeast-reductive product.
Bioscience, biotechnology, and biochemistry 2005;69(8):1589-94.
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2005: Yamauchi Satoshi; Okazaki Momotoshi; Akiyama Koichi; Sugahara Takuya; Kishida Taro; Kashiwagi Takehiro
First enantioselective synthesis of (-)- and (+)-virgatusin, tetra-substituted tetrahydrofuran lignan.
Organic & biomolecular chemistry 2005;3(9):1670-5.
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2005: Yamauchi Satoshi; Hayashi Yoshimasa; Kirikihira Takuya; Masuda Toshiya
Synthesis and antioxidant activity of olivil-type lignans.
Bioscience, biotechnology, and biochemistry 2005;69(1):113-22.
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2004: Yamauchi Satoshi; Mori Shunji; Hirai Yoshio; Kinoshita Yoshiro
Syntheses of (+)- and (-)-dihydropinidine and (+)- and (-)-epidihydropinidine by using yeast reduction of methyl (2-oxocyclohexyl)acetate.
Bioscience, biotechnology, and biochemistry 2004;68(3):676-84.
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2004: Yamauchi Satoshi; Ina Tomoko; Kirikihira Takuya; Masuda Toshiya
Synthesis and antioxidant activity of oxygenated furofuran lignans.
Bioscience, biotechnology, and biochemistry 2004;68(1):183-92.
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2003: Yamauchi Satoshi; Kinoshita Yoshihiro; Kinoshita Yoshiro
New method for synthesizing the intermediates to 5-HETE from yeast-mediated reduction products by employing Baeyer-Villiger oxidation with complete retention of enantiomeric excess.
Bioscience, biotechnology, and biochemistry 2003;67(9):1959-69.
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2003: Yamauchi Satoshi; Uno Hidemitsu
Syntheses of the stereoisomers of neolignans morinol C and D.
Organic & biomolecular chemistry 2003;1(8):1323-9.
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2003: Yamauchi Satoshi; Yamaguchi Munetoshi
Synthesis of (+)-aptosimon, a 4-oxofurofuran lignan, by erythro selective aldol condensation and stereoconvergent cyclization as the key reactions.
Bioscience, biotechnology, and biochemistry 2003;67(4):838-46.
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2002: Yamauchi Satoshi; Bando Satoshi; Kinoshita Yoshiro
Synthesis of 1,2-oxygenated 6-arylfurofuran lignan: stereoselective synthesis of (1S,2S,5R,6S)-1-hydroxysamin.
Bioscience, biotechnology, and biochemistry 2002;66(7):1495-9.
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2001: Yamauchi S; Kinoshita Y
Synthesis of cis-lactone lignan, cis-(2S,3R)-parabenzlactone, from L-arabinose.
Bioscience, biotechnology, and biochemistry 2001;65(7):1669-72.
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2001: Yamauchi S; Kinoshita Y
First stereoselective synthesis of (+)-magnostellin C, a tetrahydrofuran type of lignan bearing a chiral secondary benzyl alcohol.
Bioscience, biotechnology, and biochemistry 2001;65(7):1559-67.
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2000: Yamauchi S; Kinoshita Y
Synthesis of optically active olivil type of lignan from L-arabinose using threo-selective aldol condensation as a key reaction.
Bioscience, biotechnology, and biochemistry 2000;64(11):2320-7.
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2000: Yamauchi S; Yamamoto N; Kinoshita Y
Improved stereoselective synthesis of optically active methylene lactone, key intermediate for the synthesis of 1,2-oxidized furofuran lignan, by direct alpha-methylenation to butanolide.
Bioscience, biotechnology, and biochemistry 2000;64(10):2209-15.
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2000: Yamauchi S; Kinoshita Y
Stereoselective model synthesis of the optically active olivil type of lignan from D-xylose.
Bioscience, biotechnology, and biochemistry 2000;64(8):1563-71.
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2000: Yamauchi S; Yamamoto N; Kinoshita Y
Stereoselective synthesis of the optically active samin type of lignan from L-glutamic acid.
Bioscience, biotechnology, and biochemistry 2000;64(4):878-81.
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1998: Ganaha M; Funabiki Y; Motoki M; Yamauchi S; Kinoshita Y
Reduction of alkyl (2-oxocyclohexyl)acetates by baker's yeast.
Bioscience, biotechnology, and biochemistry 1998;62(1):181-4.
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