Monooxygenation of styrene derivatives using recombinant E. coli biocatalyst is an efficient way to prepare the corresponding oxiranes. The electronic and geometric effects of the ring substituents are described and show the relaxed specificity of the enzyme and its high stereoselectivity. © 2004 Elsevier Ltd. All rights reserved.
Monooxygenation of styrene derivatives using recombinant E. coli biocatalyst is an efficient way to prepare the corresponding oxiranes. The electronic and geometric effects of the ring substituents are described and show the relaxed specificity of the enzyme and its high stereoselectivity
Bernasconi, S., Orsini, F., Sello, G., DI GENNARO, P. (2004). Bacterial monooxygenase mediated preparation of nonracemic chiral oxiranes: Study of the effects of substituent nature and position. TETRAHEDRON-ASYMMETRY, 15(10), 1603-1606 [10.1016/j.tetasy.2004.04.005].
Bacterial monooxygenase mediated preparation of nonracemic chiral oxiranes: Study of the effects of substituent nature and position
DI GENNARO, PATRIZIA
2004
Abstract
Monooxygenation of styrene derivatives using recombinant E. coli biocatalyst is an efficient way to prepare the corresponding oxiranes. The electronic and geometric effects of the ring substituents are described and show the relaxed specificity of the enzyme and its high stereoselectivity. © 2004 Elsevier Ltd. All rights reserved.
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