Chiral Bioinspired Non-Heme Iron Complexes for Enantioselective Epoxidation of α,β-Unsaturated Ketones
文献类型:期刊论文
| 作者 | Sun W(孙伟) ; Xia CG(夏春谷) ; Hu XX(胡霄雪) ; Miao CX(苗成霞) ; Sun W(孙伟) ; Wang SF(王寿峰)
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| 刊名 | Adv. Synth. Catal.
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| 出版日期 | 2011 |
| 卷号 | 353期号:16页码:3014-3022 |
| 关键词 | chiral N4 ligand enantioselectivity epoxidation iron a,b-unsaturated carbonyl compounds |
| ISSN号 | 1615-4150 |
| 通讯作者 | 孙伟 |
| 中文摘要 | Chiral bioinspired iron complexes of N4 ligands based on the ethylenediamine backbone display remarkable levels of enantioselectivity for the first time in the asymmetric epoxidation of a,b-unsaturated ketones using hydrogen peroxide (up to 87% ee) or peracetic acid as oxidant, respectively. Notablely, isotopic labeling with H2 18O strongly demonstrated that there is a reversible water binding step prior to generation of the significant intermediate. Besides, the complex [L2FeACHTUNGTRENUNG(III)2ACHTUNGTRENUNG(m-O)ACHTUNGTRENUNG(m-CH3CO2)]3+ usually derived from the decay of the LFe(IV)=O species or thermodynamic sinks for a number of iron complexes was identified by HR-MS. In addition, the possible mechanisms were proposed and LFe(V)=O species may be the main active intermediate in the catalytic system. |
| 学科主题 | 仿生与生物催化 |
| 收录类别 | SCI |
| 资助信息 | the Chinese Academy of Sciences and National Natural Science Foundation of China (20873166 and 21073210). |
| 语种 | 英语 |
| 公开日期 | 2012-09-20 |
| 源URL | [http://210.77.64.217/handle/362003/279] ![]() |
| 专题 | 兰州化学物理研究所_OSSO国家重点实验室 |
| 通讯作者 | Sun W(孙伟); Sun W(孙伟) |
| 推荐引用方式 GB/T 7714 | Sun W,Xia CG,Hu XX,et al. Chiral Bioinspired Non-Heme Iron Complexes for Enantioselective Epoxidation of α,β-Unsaturated Ketones[J]. Adv. Synth. Catal.,2011,353(16):3014-3022. |
| APA | 孙伟,夏春谷,胡霄雪,苗成霞,孙伟,&王寿峰.(2011).Chiral Bioinspired Non-Heme Iron Complexes for Enantioselective Epoxidation of α,β-Unsaturated Ketones.Adv. Synth. Catal.,353(16),3014-3022. |
| MLA | 孙伟,et al."Chiral Bioinspired Non-Heme Iron Complexes for Enantioselective Epoxidation of α,β-Unsaturated Ketones".Adv. Synth. Catal. 353.16(2011):3014-3022. |
入库方式: OAI收割
来源:兰州化学物理研究所
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