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Short Chemoenzymatic Synthesis of S-Enantiomers of Two Systemis Fungicides (CROSBI ID 113896)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Majerić, Maja ; Avdagić, Amir ; Hameršak, Zdenko ; Šunjić, Vitomir Short Chemoenzymatic Synthesis of S-Enantiomers of Two Systemis Fungicides // Biotechnology letters, 17 (1995), 11; 1189-1194-x

Podaci o odgovornosti

Majerić, Maja ; Avdagić, Amir ; Hameršak, Zdenko ; Šunjić, Vitomir

engleski

Short Chemoenzymatic Synthesis of S-Enantiomers of Two Systemis Fungicides

2-Methyl-(4-tert-butyl)cinnamaldehyde was reduced by baker's yeast to S-3-(4-tert-butyl)-phenyl-2-propanol in high chemical and very high optical yield (99%). Chlorination and alkylation of the corresponding cyclic amines complete this short enantioselective synthesis to S-enantiomers of fenpropidine and fenpropimorph, commercialy important systemic fungicides.

Saccharomyces cerevisae; fenpropidine; fenpropimorph

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Podaci o izdanju

17 (11)

1995.

1189-1194-x

objavljeno

0141-5492

Povezanost rada

Kemija

Indeksiranost