Stereoselective chemo-enzymatic oxidation routes for (1R,3E,7E,11S,12S)-3,7,18-dolabellatriene

Frontiers in Microbiology

Volumn 6, Issue OCT, 2015, Pages

  Görner, Christian ^a   Hirte, Max ^a   Huber, Stephanie ^a   Schrepfer, Patrick ^a   Brück, Thomas ^a  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

Chemo enzymatic synthesis; Diterpenes; Dolabellanes; Epoxidation; Hydroboration

Indexed keywords

3,7,18 DOLABELLATRIENE; CYTOCHROME P450 BM3; DITERPENE; DOLABELLANE; HYDROGEN PEROXIDE; PERACETIC ACID; UNCLASSIFIED DRUG;

ANTIMICROBIAL ACTIVITY; ARTICLE; BIOCATALYSIS; BIOMASS PRODUCTION; DILOPHUS SPIRALIS; DRUG HYDROXYLATION; DRUG MANUFACTURE; DRUG SYNTHESIS; ENANTIOMERIC RATIO; EPOXIDATION; ESCHERICHIA COLI; HYDROBORATION; MOLECULAR DOCKING; OXIDATION; RECOMBINANT PLASMID; STAPHYLOCOCCUS AUREUS; STEREOCHEMISTRY;

EID: 84946841992     PISSN: None     EISSN: 1664302X     Source Type: Journal    
DOI: 10.3389/fmicb.2015.01115     Document Type: Article

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