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Satoshi Yamauchi

Faculty of Agriculture

Ehime University

3-5-7 Tarumi

Matsuyama

Japan

[email]@agr.ehime-u.ac.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Faculty of Agriculture, Ehime University, 3-5-7 Tarumi, Matsuyama, Japan. 2000 - 2009
  • Faculty of Agriculture, Ehime University. 2006

References

  1. Inhibition of the discoloration of yellowtail dark muscle by lignan. Yamauchi, S., Kishida, T., Sugahara, T., Yamawaki, M., Nishimoto, S., Shinomiya, Y., Yamamoto, T. Biosci. Biotechnol. Biochem. (2009) [Pubmed]
  2. Effect of the benzylic structure of lignan on antioxidant activity. Yamauchi, S., Sugahara, T., Matsugi, J., Someya, T., Masuda, T., Kishida, T., Akiyama, K., Maruyama, M. Biosci. Biotechnol. Biochem. (2007) [Pubmed]
  3. Determination of the stereochemistry of the tetrahydropyran sesquineolignans morinols A and B. Yamauchi, S., Sugahara, T., Akiyama, K., Maruyama, M., Kishida, T. J. Nat. Prod. (2007) [Pubmed]
  4. 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. Yamauchi, S., Nakato, T., Tsuchiya, M., Akiyama, K., Maruyama, M., Sugahara, T., Kishida, T. Biosci. Biotechnol. Biochem. (2007) [Pubmed]
  5. Radical and superoxide scavenging activities of matairesinol and oxidized matairesinol. Yamauchi, S., Sugahara, T., Nakashima, Y., Okada, A., Akiyama, K., Kishida, T., Maruyama, M., Masuda, T. Biosci. Biotechnol. Biochem. (2006) [Pubmed]
  6. Effect of benzylic oxygen on the cytotoxic activity for colon 26 cell line of phenolic lignans. Yamauchi, S., Sugahara, T., Nakashima, Y., Abe, K., Hayashi, Y., Akiyama, K., Kishida, T., Maruyama, M. Biosci. Biotechnol. Biochem. (2006) [Pubmed]
  7. Synthesis and antioxidant activity of olivil-type lignans. Yamauchi, S., Hayashi, Y., Kirikihira, T., Masuda, T. Biosci. Biotechnol. Biochem. (2005) [Pubmed]
  8. First enantioselective synthesis of (-)- and (+)-virgatusin, tetra-substituted tetrahydrofuran lignan. Yamauchi, S., Okazaki, M., Akiyama, K., Sugahara, T., Kishida, T., Kashiwagi, T. Org. Biomol. Chem. (2005) [Pubmed]
  9. Synthesis of an optically pure synthetic intermediate of aloperine from a yeast-reductive product. Yamauchi, S., Omi, Y. Biosci. Biotechnol. Biochem. (2005) [Pubmed]
  10. Effect of benzylic oxygen on the antioxidant activity of phenolic lignans. Yamauchi, S., Hayashi, Y., Nakashima, Y., Kirikihira, T., Yamada, K., Masuda, T. J. Nat. Prod. (2005) [Pubmed]
  11. Syntheses of (+)- and (-)-dihydropinidine and (+)- and (-)-epidihydropinidine by using yeast reduction of methyl (2-oxocyclohexyl)acetate. Yamauchi, S., Mori, S., Hirai, Y., Kinoshita, Y. Biosci. Biotechnol. Biochem. (2004) [Pubmed]
  12. Synthesis of (+)-aptosimon, a 4-oxofurofuran lignan, by erythro selective aldol condensation and stereoconvergent cyclization as the key reactions. Yamauchi, S., Yamaguchi, M. Biosci. Biotechnol. Biochem. (2003) [Pubmed]
  13. Syntheses of the stereoisomers of neolignans morinol C and D. Yamauchi, S., Uno, H. Org. Biomol. Chem. (2003) [Pubmed]
  14. 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. Yamauchi, S., Kinoshita, Y., Kinoshita, Y. Biosci. Biotechnol. Biochem. (2003) [Pubmed]
  15. Synthesis of 1,2-oxygenated 6-arylfurofuran lignan: stereoselective synthesis of (1S,2S,5R,6S)-1-hydroxysamin. Yamauchi, S., Bando, S., Kinoshita, Y. Biosci. Biotechnol. Biochem. (2002) [Pubmed]
  16. First stereoselective synthesis of (+)-magnostellin C, a tetrahydrofuran type of lignan bearing a chiral secondary benzyl alcohol. Yamauchi, S., Kinoshita, Y. Biosci. Biotechnol. Biochem. (2001) [Pubmed]
  17. Synthesis of cis-lactone lignan, cis-(2S,3R)-parabenzlactone, from L-arabinose. Yamauchi, S., Kinoshita, Y. Biosci. Biotechnol. Biochem. (2001) [Pubmed]
  18. Stereoselective synthesis of the optically active samin type of lignan from L-glutamic acid. Yamauchi, S., Yamamoto, N., Kinoshita, Y. Biosci. Biotechnol. Biochem. (2000) [Pubmed]
  19. Stereoselective model synthesis of the optically active olivil type of lignan from D-xylose. Yamauchi, S., Kinoshita, Y. Biosci. Biotechnol. Biochem. (2000) [Pubmed]
  20. 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. Yamauchi, S., Yamamoto, N., Kinoshita, Y. Biosci. Biotechnol. Biochem. (2000) [Pubmed]
  21. Synthesis of optically active olivil type of lignan from L-arabinose using threo-selective aldol condensation as a key reaction. Yamauchi, S., Kinoshita, Y. Biosci. Biotechnol. Biochem. (2000) [Pubmed]
 
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