DICP OpenIR
An efficient enantioselective method for asymmetiric Michael addition of nitroalkanes to alpha,beta-unsaturated aldehydes
Wang, Yongcan3; Li, Pengfei3; Liang, Xinmiao1,3; Zhang, Tony Y.2; Ye, Jinxing1,3
刊名CHEMICAL COMMUNICATIONS
2008-03-14
DOI10.1039/b717000a
10页:1232-1234
收录类别SCI ; CCR
文章类型Article
WOS标题词Science & Technology ; Physical Sciences
类目[WOS]Chemistry, Multidisciplinary
研究领域[WOS]Chemistry
关键词[WOS]ORGANOCATALYTIC CONJUGATE ADDITION ; BACLOFEN ; CATALYST ; ENONES ; ALDOL ; HYDROPHOSPHINATION ; ENANTIOMERS ; ETHER
英文摘要The addition of nitroalkanes to alpha,beta-unsaturated aldehydes under the catalysis of (S)-2-(dipheny](trimethylsilyloxy)methyl)pyrrolidine and lithium acetate as additive afforded gamma-nitroaldehydes in good yield and up to 97% ee.
语种英语
WOS记录号WOS:000254579500023
引用统计
文献类型期刊论文
条目标识符http://cas-ir.dicp.ac.cn/handle/321008/140955
专题中国科学院大连化学物理研究所
作者单位1.E China Univ Sci & Technol, Sch Pharm, Shanghai 200237, Peoples R China
2.Eli Lilly & Co, Indianapolis, IN 46285 USA
3.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
推荐引用方式
GB/T 7714
Wang, Yongcan,Li, Pengfei,Liang, Xinmiao,et al. An efficient enantioselective method for asymmetiric Michael addition of nitroalkanes to alpha,beta-unsaturated aldehydes[J]. CHEMICAL COMMUNICATIONS,2008(10):1232-1234.
APA Wang, Yongcan,Li, Pengfei,Liang, Xinmiao,Zhang, Tony Y.,&Ye, Jinxing.(2008).An efficient enantioselective method for asymmetiric Michael addition of nitroalkanes to alpha,beta-unsaturated aldehydes.CHEMICAL COMMUNICATIONS(10),1232-1234.
MLA Wang, Yongcan,et al."An efficient enantioselective method for asymmetiric Michael addition of nitroalkanes to alpha,beta-unsaturated aldehydes".CHEMICAL COMMUNICATIONS .10(2008):1232-1234.
条目包含的文件
条目无相关文件。
个性服务
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
谷歌学术
谷歌学术中相似的文章
[Wang, Yongcan]的文章
[Li, Pengfei]的文章
[Liang, Xinmiao]的文章
百度学术
百度学术中相似的文章
[Wang, Yongcan]的文章
[Li, Pengfei]的文章
[Liang, Xinmiao]的文章
必应学术
必应学术中相似的文章
[Wang, Yongcan]的文章
[Li, Pengfei]的文章
[Liang, Xinmiao]的文章
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

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。