Highly Stereoselective and One-Pot Synthesis of Tetra-substituted Monofluoroalkenes with Aldehydes and Fluorobis(phenylsulfonyl)methane
Shen X(沈晓) ; Ni CF(倪传法) ; Hu JB(胡金波)
刊名Chin. J. Chem.
2013
卷号31期号:7页码:878-884
ISSN号1001-604X
其他题名从醛和一氟二苯磺酰基甲烷出发高立体选择性地一锅法合成四取代的单氟烯烃
通讯作者胡金波
英文摘要A highly stereoselective synthesis of tetrasubstituted monofluoroalkenes with aldehydes and fluorobis(phenylsulfonyl)methane (FBSM) in one pot has been developed. The reaction was amenable to para- and meta-substituted aryl aldehydes, 2-naphthaldehyde, an
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/cjoc.201300365
语种英语
WOS记录号WOS:000327700000004
公开日期2014-10-15
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/29209]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
推荐引用方式
GB/T 7714
Shen X,Ni CF,Hu JB. Highly Stereoselective and One-Pot Synthesis of Tetra-substituted Monofluoroalkenes with Aldehydes and Fluorobis(phenylsulfonyl)methane[J]. Chin. J. Chem.,2013,31(7):878-884.
APA 沈晓,倪传法,&胡金波.(2013).Highly Stereoselective and One-Pot Synthesis of Tetra-substituted Monofluoroalkenes with Aldehydes and Fluorobis(phenylsulfonyl)methane.Chin. J. Chem.,31(7),878-884.
MLA 沈晓,et al."Highly Stereoselective and One-Pot Synthesis of Tetra-substituted Monofluoroalkenes with Aldehydes and Fluorobis(phenylsulfonyl)methane".Chin. J. Chem. 31.7(2013):878-884.
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