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Tailoring chemoenzymatic oxidation via in situ peracids

Journal Article · · Organic and Biomolecular Chemistry
DOI:https://doi.org/10.1039/c9ob01814j· OSTI ID:1799473
 [1];  [2];  [2];  [3];  [2]
  1. Univ. of California, San Diego, CA (United States). Dept. of Chemistry and Biochemistry; OSTI
  2. Univ. of California, San Diego, CA (United States). Dept. of Chemistry and Biochemistry
  3. Univ. of California, San Diego, CA (United States). Dept. of Chemistry and Biochemistry; Univ. Montpellier (France). UMR IATE. Montpellier SupAgro. INRA

Epoxidation chemistry often suffers from the challenging handling of peracids and thus requires in situ preparation. Here, we describe a two-phase enzymatic system that allows the effective generation of peracids and directly translate their activity to the epoxidation of olefins. We demonstrate the approach by application to lipid and olefin epoxidation as well as sulfide oxidation. These methods offer useful applications to synthetic modifications and scalable green processes.

Research Organization:
Univ. of California, San Diego, CA (United States)
Sponsoring Organization:
USDOE Office of Energy Efficiency and Renewable Energy (EERE), Transportation Office. Bioenergy Technologies Office
Grant/Contract Number:
EE0008246
OSTI ID:
1799473
Alternate ID(s):
OSTI ID: 1571831
Journal Information:
Organic and Biomolecular Chemistry, Journal Name: Organic and Biomolecular Chemistry Journal Issue: 43 Vol. 17; ISSN 1477-0520
Publisher:
Royal Society of ChemistryCopyright Statement
Country of Publication:
United States
Language:
English

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