中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Iridium-Catalyzed Asymmetric Allylic Etherification and Ring-Closing Metathesis Reaction for Enantioselective Synthesis of Chromene and 2,5-Dihydrobenzo[b]oxepine Derivatives

文献类型:期刊论文

作者He H(贺虎) ; Ye KY(叶克印) ; Wu QF(武庆锋) ; Dai LX(戴立信) ; You SL(游书力)
刊名Adv. Synth. Catal.
出版日期2012
卷号354期号:6页码:1084-1094
ISSN号1615-4150
其他题名通过铱催化的不对称烯丙基醚化和关环复分解(RCM)反应实现的苯并吡喃和 2,5-Dihydrobenzo [b]oxepine衍生物的手性合成
通讯作者游书力
英文摘要Iridium-catalyzed asymmetric etherifications of allylic carbonates with 2-vinylphenols and 2-allylphenols were realized. With a catalyst generated from 2 mol% of [Ir(cod)Cl]2 (cod=cycloocta-1,5-diene) and 4 mol% of the phosphoramidite ligand L2, the etherification products were obtained in excellent ees and then subjected to the ring-closing metathesis reaction providing an efficient synthesis of enantioenriched 2H-chromene and 2,5-dihydrobenzo[b]oxepine derivatives.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/adsc.201100809
语种英语
WOS记录号WOS:000302936000018
公开日期2013-08-22
源URL[http://202.127.28.38/handle/331003/27999]  
专题上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式
GB/T 7714
He H,Ye KY,Wu QF,et al. Iridium-Catalyzed Asymmetric Allylic Etherification and Ring-Closing Metathesis Reaction for Enantioselective Synthesis of Chromene and 2,5-Dihydrobenzo[b]oxepine Derivatives[J]. Adv. Synth. Catal.,2012,354(6):1084-1094.
APA 贺虎,叶克印,武庆锋,戴立信,&游书力.(2012).Iridium-Catalyzed Asymmetric Allylic Etherification and Ring-Closing Metathesis Reaction for Enantioselective Synthesis of Chromene and 2,5-Dihydrobenzo[b]oxepine Derivatives.Adv. Synth. Catal.,354(6),1084-1094.
MLA 贺虎,et al."Iridium-Catalyzed Asymmetric Allylic Etherification and Ring-Closing Metathesis Reaction for Enantioselective Synthesis of Chromene and 2,5-Dihydrobenzo[b]oxepine Derivatives".Adv. Synth. Catal. 354.6(2012):1084-1094.

入库方式: OAI收割

来源:上海有机化学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。