Regio- and stereoselective hydroxylation of 10-undecenoic acid with a light-driven P450 BM3 biocatalyst yielding a valuable synthon for natural product synthesis

Bioorganic and Medicinal Chemistry

Volumn 22, Issue 20, 2014, Pages 5687-5691

  Kato, Mallory ^a   Nguyen, Daniel ^a   Gonzalez, Melissa ^a   Cortez, Alejandro ^a   Mullen, Sarah E ^a   Cheruzel, Lionel E ^a  

^a SAN JOSE STATE UNIVERSITY   (United States)

Author keywords

Allylic oxidation (R) 9 Hydroxy 10 undecenoic acid; Light driven; Natural product synthesis; P450 BM3 biocatalyst; Stereoselective hydroxylation

Indexed keywords

10 UNDECENOIC ACID; 9 HYDROXY 10 UNDECENOIC ACID; CYTOCHROME P450 BM3; NATURAL PRODUCT; UNCLASSIFIED DRUG; BACTERIAL PROTEIN; BIOLOGICAL PRODUCT; CYTOCHROME P450; FLAVOCYTOCHROME P450 BM3 MONOXYGENASES; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE FERRIHEMOPROTEIN REDUCTASE;

ARTICLE; BIOCATALYST; DRUG DETERMINATION; DRUG STRUCTURE; DRUG SYNTHESIS; ENZYME MECHANISM; ENZYME METABOLISM; ENZYME SUBSTRATE; EPOXIDATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYBRID; HYDROXYLATION; LIGHT; REGIOSELECTIVITY; STEREOCHEMISTRY; BIOCATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; ISOLATION AND PURIFICATION; METABOLISM; STEREOISOMERISM;

BACTERIAL PROTEINS; BIOCATALYSIS; BIOLOGICAL PRODUCTS; CYTOCHROME P-450 ENZYME SYSTEM; HYDROXYLATION; LIGHT; MODELS, MOLECULAR; MOLECULAR STRUCTURE; NADPH-FERRIHEMOPROTEIN REDUCTASE; STEREOISOMERISM; UNDECYLENIC ACIDS;

EID: 84908555867     PISSN: 09680896     EISSN: 14643391     Source Type: Journal    
DOI: 10.1016/j.bmc.2014.05.046     Document Type: Article

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