C-F Bond Cleavage by Intramolecular S(N)2 Reaction of Alkyl Fluorides with O- and N-Nucleophiles
Zhang LJ(张来俊) ; Zhang W(张伟) ; Liu J(刘俊) ; Hu JB(胡金波)
刊名J. Org. Chem.
2009
卷号74期号:7页码:2850-2853
ISSN号0022-3263
其他题名利用氧-和氮-亲核试剂对烷基氟化物的SN2反应来实现C-F键断裂
通讯作者胡金波
英文摘要The nucleophilic substitution of alkyl fluorides was achieved in the intramolecular reactions with O- and N-nucleophiles. The intramolecular defluorinative cyclization reaction was influenced by the nature of nucleophiles, the size of the ring to be formed, and the comformational rigidity of the precursors. Intermolecular nucleophilic substitution reactions of alkyl fluorides under similar reaction conditions were found to be difficult. The stereochemistry study of the current C-F bond cleavage reaction showed a complete configurational inversion, which supports an intramolecular S(N)2 reaction mechanism.
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/jo802819p
语种英语
WOS记录号WOS:000264627400030
公开日期2013-03-11
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/24049]  
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
Zhang LJ,Zhang W,Liu J,et al. C-F Bond Cleavage by Intramolecular S(N)2 Reaction of Alkyl Fluorides with O- and N-Nucleophiles[J]. J. Org. Chem.,2009,74(7):2850-2853.
APA 张来俊,张伟,刘俊,&胡金波.(2009).C-F Bond Cleavage by Intramolecular S(N)2 Reaction of Alkyl Fluorides with O- and N-Nucleophiles.J. Org. Chem.,74(7),2850-2853.
MLA 张来俊,et al."C-F Bond Cleavage by Intramolecular S(N)2 Reaction of Alkyl Fluorides with O- and N-Nucleophiles".J. Org. Chem. 74.7(2009):2850-2853.
个性服务
查看访问统计
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。


©版权所有 ©2017 CSpace - Powered by CSpace