Stereochemistry of the enzymatic reduction of 2-(4-methoxybenzyl)-1-cyclohexanone by solanum aviculare cells in vitro

Biocatalysis and Biotransformation

Volumn 2, Issue 4, 1989, Pages 265-272

  Vanek, Tomáscaron ^a   Wimmer, Zdeněk ^a   Macek, Tomáscaron ^a   Šaman, David ^a   Svatoš, Aleš ^a   Romaňuk, Miroslav ^a  

^a INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

Author keywords

2 (4 methoxybenzyl) 1 cyclohexanol; 2 (4 methoxybenzyl) 1 cyclohexanone; Biotransformation by plant cells; Enzymatic reduction; Solanum aviculare; Stereochemistry of reduction

Indexed keywords

EID: 2442438083     PISSN: 10242422     EISSN: None     Source Type: Journal    
DOI: 10.3109/10242428908992036     Document Type: Article

References (10)

1. Pyridinium chlorochromate. An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compounds
2. Oxidoreduction between cycloalkanols and the corresponding cycloalkanones in the cultured cells of Nicotiana tabacum. Simulation of the time courses in the oxidoreduction
3. Organic growth factor requirements of tobacco tissue cultures
4. Poroporo (Solanum aviculare FORST., Solanum laciniatum AIT.): In vitro Culture and the Production of Solasodine
5. A revised medium for rapid growth and bioassays with tobacco tissue cultures
6. Direct esterification of α-methoxy-α-(trifiuoromethyl)phenylacetic acid
7. 13C NMR chemical shift of the carbonyl carbon
8. Biotransformation of 2-(4-methoxybenzyl)-1-cyclohexanone by means of Saccharomyces cerevisiae
9. Biotransformation of 2-(4-methoxybenzyl)-1-cyclohexanone by cell cultures of Solanum aviculare