4.7 Article

Asymmetric epoxidation of alkenes and benzylic hydroxylation with P450tol monooxygenase from Rhodococcus coprophilus TC-2

Journal

CHEMICAL COMMUNICATIONS
Volume 50, Issue 63, Pages 8771-8774

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4cc03491k

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Funding

  1. GlaxoSmithKline
  2. Singapore Economic Development Board [279-000-331-592]

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P450tol monooxygenase was discovered as a unique and highly enantioselective enzyme for asymmetric epoxidation of some terminal alkenes containing electron-withdrawing groups and benzylic hydroxylation of several ethylbenzenes giving the corresponding useful and valuable products, such as (R)-2- and 3-substituted styrene oxides, (S)-4-substituted styrene oxides, and (S)-benzylic alcohols, in high ee.

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