Eine biokatalytische Henry‐Reaktion – die Hydroxynitrillyase aus Hevea brasiliensis katalysiert auch Nitroaldolreaktionen

作者: Thomas Purkarthofer , Karl Gruber , Mandana Gruber-Khadjawi , Kerstin Waich , Wolfgang Skranc

DOI: 10.1002/ANGE.200504230

关键词:

摘要:

参考文章(40)
Martin H. Fechter, Herfried Griengl, Formation of C ? C Bonds: Enzymatic Synthesis of Cyanohydrins Enzyme Catalysis in Organic Synthesis: A Comprehensive Handbook, Second Edition. pp. 974- 989 ,(2008) , 10.1002/9783527618262.CH14B
Takashi Ooi, Kanae Doda, Keiji Maruoka, Designer chiral quaternary ammonium bifluorides as an efficient catalyst for asymmetric nitroaldol reaction of silyl nitronates with aromatic aldehydes. Journal of the American Chemical Society. ,vol. 125, pp. 2054- 2055 ,(2003) , 10.1021/JA029660P
David A. Evans, Daniel Seidel, Magnus Rueping, Hon Wai Lam, Jared T. Shaw, C. Wade Downey, A new copper acetate-bis(oxazoline)-catalyzed, enantioselective Henry reaction Journal of the American Chemical Society. ,vol. 125, pp. 12692- 12693 ,(2003) , 10.1021/JA0373871
Masakatsu Shibasaki, Naoki Yoshikawa, Lanthanide complexes in multifunctional asymmetric catalysis. Chemical Reviews. ,vol. 102, pp. 2187- 2209 ,(2002) , 10.1021/CR010297Z
Richard M. Stephenson, Mutual solubilities: water-ketones, water-ethers, and water-gasoline-alcohols Journal of Chemical & Engineering Data. ,vol. 37, pp. 80- 95 ,(1992) , 10.1021/JE00005A024
K. Gruber, M. Gugganig, U. G. Wagner, C. Kratky, Atomic Resolution Crystal Structure of Hydroxynitrile Lyase from Hevea Brasiliensis Biological Chemistry. ,vol. 380, pp. 993- 1000 ,(1999) , 10.1515/BC.1999.123
Frederick G. Bordwell, William J. Boyle, Judith A. Hautala, K. C. Yee, Broensted coefficients larger than 1 and less than 0 for proton removal from carbon acids Journal of the American Chemical Society. ,vol. 91, pp. 4002- 4003 ,(1969) , 10.1021/JA01042A082
Monica Sharma, Nitya Nand Sharma, Tek Chand Bhalla, Hydroxynitrile lyases: At the interface of biology and chemistry Enzyme and Microbial Technology. ,vol. 37, pp. 279- 294 ,(2005) , 10.1016/J.ENZMICTEC.2005.04.013
Karl Gruber, Günter Gartler, Barbara Krammer, Helmut Schwab, Christoph Kratky, Reaction mechanism of hydroxynitrile lyases of the alpha/beta-hydrolase superfamily: the three-dimensional structure of the transient enzyme-substrate complex certifies the crucial role of LYS236. Journal of Biological Chemistry. ,vol. 279, pp. 20501- 20510 ,(2004) , 10.1074/JBC.M401575200