Theoretical study of regioselectivity in the synthesis of spiro [pyrrolidine-2,3'-oxindole] compounds by [3+2] cycloaddition | |
Chen, Gang; Yang, Jing; Gao, Suo; Zhang, Yu; Hao, Xiaojiang | |
刊名 | RESEARCH ON CHEMICAL INTERMEDIATES |
2015-07-01 | |
卷号 | 41期号:7页码:4987-4996 |
关键词 | Regioselectivity Theoretical Spiro-oxindole [3+2] Cycloaddition |
英文摘要 | Study of the structures of a series of spiro [pyrrolidine-2,3'-oxindole] derivatives synthesized by [3+2] cycloaddition reaction of isatin, alpha-amino acids, and beta-substituted phenylethylenes revealed the regioselectivity of the reaction was completely novel. The reaction mechanism for [3+2] cycloaddition of oxindole azomethine ylide and the beta-substituted phenylethylenes was calculated by use of density functional theory with the B3LYP functional and different basis sets. The results show that the regioselectivity of this [3+2] cycloaddition reaction is kinetically controlled, which agrees with experimental results. |
类目[WOS] | Chemistry, Multidisciplinary |
研究领域[WOS] | Chemistry |
关键词[WOS] | 1,3-DIPOLAR CYCLOADDITION ; DERIVATIVES |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000356608700072 |
内容类型 | 期刊论文 |
源URL | [http://ir.kib.ac.cn/handle/151853/24975] |
专题 | 昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室 |
推荐引用方式 GB/T 7714 | Chen, Gang,Yang, Jing,Gao, Suo,et al. Theoretical study of regioselectivity in the synthesis of spiro [pyrrolidine-2,3'-oxindole] compounds by [3+2] cycloaddition[J]. RESEARCH ON CHEMICAL INTERMEDIATES,2015,41(7):4987-4996. |
APA | Chen, Gang,Yang, Jing,Gao, Suo,Zhang, Yu,&Hao, Xiaojiang.(2015).Theoretical study of regioselectivity in the synthesis of spiro [pyrrolidine-2,3'-oxindole] compounds by [3+2] cycloaddition.RESEARCH ON CHEMICAL INTERMEDIATES,41(7),4987-4996. |
MLA | Chen, Gang,et al."Theoretical study of regioselectivity in the synthesis of spiro [pyrrolidine-2,3'-oxindole] compounds by [3+2] cycloaddition".RESEARCH ON CHEMICAL INTERMEDIATES 41.7(2015):4987-4996. |
个性服务 |
查看访问统计 |
相关权益政策 |
暂无数据 |
收藏/分享 |
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。
修改评论