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Browsing Makale Koleksiyonu by Author "Kurbanoğlu, Namudar İzzet"

Now showing items 1-5 of 5

Asymmetric reduction of acetophenone analogues by Alternaria alternata using ram horn peptone

Kurbanoğlu, Namudar İzzet; Kılıç, Harun (PERGAMON-ELSEVIER SCIENCE LTD, 2007)

Alternaria alternata EBK-4 fungus isolated from a plant sample was evaluated for the asymmetric reduction of acetophenone analogues. In a previous study, this isolate was used for the reduction of acetophenone to 1-phenylethanol ...
Enantioselective reduction of substituted acetophenones by Aspergillus niger

Kurbanoğlu, Namudar İzzet; Kılıç, Harun (PERGAMON-ELSEVIER SCIENCE LTD, 2007)

Fourteen strains of Aspergillus niger were isolated from soil samples. These isolates were evaluated for tile reduction of acetophenone to 1-phenylethanol. Among the tested isolates, whole cells of the A. niger EBK-9 isolate ...
Production of (R)-1-phenylethanols Through Bioreduction of Acetophenones by a New Fungus Isolate Trichothecium roseum

Taşkın, Mehmet Fatih; Kurbanoğlu, Namudar İzzet; Kılıç, Harun (WILEY, 2010)

A total of 120 fungal strains were isolated from soil samples and evaluated in the bioreduction of substituted acetophenones to the corresponding (R)-alcohols. Among these strains, isolate Trichothecium roseum EBK-18 was ...
Production of (S)-(-)-1-(1'-Napthyl) Ethanol by Rhodotorula glutinis Isolate Using Ram Horn Peptone

Kurbanoğlu, Namudar İzzet; Taşkın, Mehmet Fatih; Kılıç, Harun (SCIENTIFIC TECHNICAL RESEARCH COUNCIL TURKEY-TUBITAK, 2008)

The bioreduction of 1-acetonaphthone 1 by locally isolated Rhodotorula glutinis strains using ram horn peptone (RHP) gave (S)-(-)-1-(1'-naphthyl) ethanol ( 2), an important pharmaceutical intermediate. R. glutinis strains ...
Stereospecific synthesis of a DL-gala-aminoquercitol derivative

Kurbanoğlu, Namudar İzzet; Kılıç, Harun; Balci, Mustafa (PERGAMON-ELSEVIER SCIENCE LTD, 2010)

A new aminoquercitol derivative was synthesized starting from 1,4-cyclohexadiene. Photooxygenation of cyclohexa-1,4-diene afforded anti-2,3-dioxabicyclo[2.2.2]oct-7-en-5-yl hydroperoxicle as the main product. The formed ...