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Small molecule activation and biomimetic catalysis
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Asymmetric bioreduction of substituted acenaphthenequinones using plant enzymatic systems: A novel strategy for the preparation of (+)- and (-)-mono hydroxyacenaphthenones
Release time:2019-03-10 Hits:
Indexed by: 期刊论文
First Author: Tong, Lian Peng
Correspondence Author: Cui, JN (reprint author), Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116012, Peoples R China.
Co-author: Cui, Jing Nan,Ren, Wei Min,Wang, Xing Yong,Qian, Xu Hong
Date of Publication: 2008-10-01
Journal: CHINESE CHEMICAL LETTERS
Included Journals: SCIE、ISTIC、Scopus
Document Type: J
Volume: 19
Issue: 10
Page Number: 1179-1182
ISSN No.: 1001-8417
Key Words: Bioreduction; Plant enzymes; Acenaphthenequinone; Chiral hydroxyacenaphthenone
Abstract: Regio- and enantioselective reduction of substituted acenaphthenequinones were conducted under mild reaction conditions using plant enzymatic systems. A screening of 15 plants allowed the selection of two suitable plants fulfilling enantiocomplementarity. The (+)- and (-)-mono hydroxyacenaphthenones were achieved with high conversion and good enantiomeric purity using peach (Prunus persica (L.) Batsch., conversion 98%, 71% ee) and carrot (Daucus carota L., conversion 95%, 81% ee), respectively. (C) 2008 Jing Nan Cui. Published by Elsevier B. V. on behalf of Chinese Chemical Society. All rights reserved.
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