33
Views
4
CrossRef citations to date
0
Altmetric
SHORT COMMUNICATION

Synthesis of (R)-2-trimethylsilyl-2-hydroxyl-propionitrile catalyzed by (R)-hydroxynitrile lyase from Prunus japonica seed meal

, &
Pages 453-456 | Received 18 Oct 2004, Published online: 11 Jul 2009

References

  • Effenberger F, Förster S, Wajant H. Hydroxynitrile lyases in stereoselective catalysis. Curr Opin Biotechnol 2000; 11: 532–539
  • Gerrits PJ, Willeman WF, Straathof AJJ, Heijnen JJ, Brussee J, van der Gen A. Mass transfer limitation as a tool to enhance the enantiomeric excess in the enzymatic synthesis of chiral cyanohydrins. J Mol Catal B: Enzym 2001; 15: 111–121
  • Gotor V. Lipases and (R)-oxynitrilase:useful tools in organic synthesis. J Biotechnol 2002; 96: 35–42
  • Harada, T, Hayashiya, T, Wada, I, Iwa-ake, N, Oku, A. 1996. Enantioselective functionalization of prochiral diols via chiral spiroketals: preparation of optically pure 2-substituted 1,3-propanediol derivatives and asymmetric synthesis of chroma ring and side chain of α-tocopherol. J Am Chem Soc, 109:527–532.
  • Kawamoto T, Yamanaka H, Tanaka A. Enzymatic preparation of optically active silicon-containing amino acids and their application. Appl Biochem Biotech 2000; 88: 17–22
  • Kiljunen E, Kanerva LT. (R)- and (S)-Cyanohydrins using oxynitrilases in whole cells. Tetrahedron: Asymmetry 1996; 7: 1105–1116
  • Kiljunen E, Kanerva LT. Approach to (R)- and (S)-kentone cyanohydrins using almond and apple meal as the source of (R)-oxynitrilase. Tetrahedron: Asymmetry 1997; 8: 1551–1557
  • Li N, Zong MH, Liu C, Peng HS, Wu HC. (R)-oxynitrilase-catalysed synthesis of chiral silicon-containing aliphatic (R)-ketone-cyanohydrins. Biotechnol Lett 2003; 25: 219–222
  • Li N, Zong MH, Peng HS, Wu HC, Liu C. (R)-Oxynitrilase-catalyzed synthesis of (R)-2-trimethylsilyl-2-hydroxyl-ethylcyanide. J Mol Catal B: Enzym 2003; 22: 7–12
  • Mori K. Synthesis of optically active pheromones. Tetrahedron 1989; 45: 3233–3298
  • Zani P. Biotransformations of organosilicon compounds: enantioselective reduction of acyl silanes by means of baker's yeast. J Mol Catal B: Enzym 2001; 11: 279–285
  • Zong MH, Fukui T, Kawamoto T, Tanaka A. Bioconversion of organosilicon compounds by horse liver alcohol dehydrogenase: The role of silicon atom in enzymatic reactions. Appl Microbiol Biotechnol 1991; 36: 40–43

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.