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BIOLOGICAL INFO
Solubility:
Water: 29g/L (20°C)
REVIEW The Arthrobacter sp. is able to grow with (+ I-,(-)-1-phenylethanol or the racemic mixture as sole source of carbon. Growth is most rapid with the (-)-isomer, doubling time 12 h. Lipases show good activity and, in some cases, improved enantioselectivity when employed in pure ionic liquids for dynamic kinetic resolution of 1-phenylethanol by transesterification.
REFERENCES
[1]
Roger E. Cripps,; Peter W. Trudgill,; John G. Whateley. The Metabolism of 1-Phenylethanol and Acetophenone by Nocardia T5 and an Arthrobacter Species. European Journal of Biochemistry. 1978, 86 (1), 175-186.
[2]
Priska Hubera,; Svetoslav Bratovanova,; Stefan Bienz,; Christoph Syldatk,; Markus Pietzsch.Chiral silicon groups as auxiliaries for enantioselective synthesis: access to optically active silanes by biotransformation and the enantiospecific preparation of (R)-(+)-1-phenylethanol . Tetrahedron: Asymmetry. year of publication , 7(1), 69-78.
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