New oxyfunctionalization capabilities for. omega.-hydroxylases. Asymmetric aliphatic sulfoxidation and branched ether demethylation
AG Katopodis, HA Smith, SW May
Index: Katopodis, Andreas G.; Smith, Homer A.; May, Sheldon W. Journal of the American Chemical Society, 1988 , vol. 110, # 3 p. 897 - 899
Full Text: HTML
Citation Number: 49
Abstract
Abstract: Due to inherent difficulties in the chemical generation of aliphatic synthons, the stereo-and regioselective oxyfunctionalization of simple aliphatic substrates represents an area where chemical applications of biocatalysis would be particularly useful. The hydrocarbon monooxygenase from Pseudomonas oleouorans is a prototypical" w- hydroxylase" known to carry out hydroxylation at the terminal methyl of alkanes as well as ...
Related Articles:
[Katz, Howard Edan; Starnes, William H. Journal of Organic Chemistry, 1984 , vol. 49, # 15 p. 2758 - 2761]
[Katz, Howard Edan; Starnes, William H. Journal of Organic Chemistry, 1984 , vol. 49, # 15 p. 2758 - 2761]
Alkenylcopper Derivatives; 221, 2. Stereoselective Synthesis of Allylic Thioethers
[Germon, C.; Alexakis, A.; Normant, J. F. Synthesis, 1984 , # 1 p. 43 - 46]
[Katz, Howard Edan; Starnes, William H. Journal of Organic Chemistry, 1984 , vol. 49, # 15 p. 2758 - 2761]