SCOPUS 정보 검색 플랫폼

Volumn , Issue 5, 2002, Pages 700-702

Microbial Baeyer-Villiger oxidation of bicyclo[4.3.0]ketones by two recombinant E. coli strains. A novel access to indole alkaloids

(4) Mihovilovic, Marko D a Müller, Bernhard a Kayser, Margaret M b Stanetty, Peter a

a VIENNA UNIVERSITY OF TECHNOLOGY (Austria)

b UNIVERSITY OF NEW BRUNSWICK (Canada)

Author keywords

Baeyer Villiger oxidation; Biocatalysis; Enantioselectivity; Indole alkaloids; Monooxygenase; Recombinant whole cell biotransformation

Indexed keywords

BICYCLO COMPOUND; INDOLE ALKALOID; KETONE DERIVATIVE; LACTONE DERIVATIVE; UNSPECIFIC MONOOXYGENASE;

ACINETOBACTER; ARTICLE; BIOCATALYST; BIOTRANSFORMATION; ENANTIOMER; ESCHERICHIA COLI; NONHUMAN; OXIDATION; PSEUDOMONAS;

EID: 0036256148 PISSN: 09365214 EISSN: None Source Type: Journal
DOI: 10.1055/s-2002-25340 Document Type: Article

Times cited : (37)

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- note

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