Chemo-enzymatic enantio-convergent asymmetric synthesis of (R)-(+)-Marmin

Tetrahedron

Volumn 60, Issue 3, 2004, Pages 583-588

  Edegger, Klaus ^a   Mayer, Sandra F ^a   Steinreiber, Andreas ^a   Faber, Kurt ^a  

^a UNIVERSITY OF GRAZ   (Austria)

Author keywords

(R) (+) Marmin; Biotransformation; Epoxide hydrolase; Rhodococcus; Streptomyces

Indexed keywords

3 (5 CHLORO 3 METHYLPENT 3 ENYL) 2,2 DIMETHYLOXIRANE; 3,7 DIMETHYLOCTEN 1,6,7 TRIOL; 7 (10,11 DIHYDROXY 3,7,11 TRIMETHYLDODECADIENYLOXY)CHROMEN 2 ONE; 7 (3,7,11 TRIMETHYLDODECATRIENYLOXY)CHROMEN 2 ONE; 7 (6,7 DIHYDROXY 3,7 DIMETHYLOCTENYLOXY)CHROMEN 2 ONE; 7 (7 HYDROXY 3,7 DIMETHYL 6 OXOOCTENYLOXY)CHROMEN 2 ONE; 7 [5 (3,3 DIMETHYLOXIRANYL) 3 METHYLPENTENYLOXYL]CHROMEN 2 ONE; 7 [9 (3,3 DIMETHYLOXIRANYL) 3,7 DIMETHYLNONADIENYLOXYL]CHROMEN 2 ONE; 8 CHLORO 2,6 DIMETHYLOCTEN 2,3 DIOL; CHROMENE DERIVATIVE; COUMARIN; EPOXIDE HYDROLASE; ETHYLENE OXIDE DERIVATIVE; MARMIN; OXYGEN; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

AEROBIC METABOLISM; ARTICLE; ATMOSPHERE; BIOCATALYST; BIOTRANSFORMATION; ENZYME ACTIVITY; HYDROLYSIS; NONHUMAN; PRIORITY JOURNAL; RHODOCOCCUS; STREPTOCOCCUS; SYNTHESIS;

RHODOCOCCUS; STAPHYLOCOCCUS PHAGE 3A; STREPTOMYCES;

EID: 0347595488     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2003.10.106     Document Type: Article

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