Oxadiazepine Synthesis by Formal [4+3] Cycloaddition of o-Chloromethyl Arylsulfonamides with Nitrones Promoted by NaHCO3 | |
Zhang, Xiaoke1,2; Pan, Yang1,2; Liang, Peng1,2; Pang, Lu2; Ma, Xiaofeng1,2; Jiao, Wei2; Shao, Huawu2 | |
刊名 | ADVANCED SYNTHESIS & CATALYSIS |
2018 | |
卷号 | 360期号:16页码:3015-3019 |
关键词 | arylsulfonamides cycloaddition nitrone oxadiazepine |
ISSN号 | 1615-4150 |
DOI | 10.1002/adsc.201800663 |
产权排序 | 1 |
文献子类 | Article |
英文摘要 | An effective and facile method for the synthesis of highly substituted 1,2,3,5-tetrahydrobenzo[e][1,2,4]-oxadiazepines is described. A formal [4+3] cycloaddition of N-(2-(chloromethyl) phenyl) amides with nitrones afforded benzo[e][1,2,4]-oxadiazepine derivatives with high atom economy and excellent yields (up to 97%). |
学科主题 | Organic Chemistry ; Polymer Science |
URL标识 | 查看原文 |
WOS关键词 | 1,2-CYCLOPROPANATED SUGARS ; N-(ORTHO-CHLOROMETHYL)ARYL AMIDES ; STEREOSELECTIVE-SYNTHESIS ; CONVENIENT SYNTHESIS ; ASYMMETRIC-SYNTHESIS ; SMALL-MOLECULE ; SULFUR YLIDES ; DERIVATIVES ; DISCOVERY ; 3,1,5-BENZOXADIAZEPINES |
WOS研究方向 | Chemistry |
语种 | 英语 |
出版者 | WILEY-V C H VERLAG GMBH |
WOS记录号 | WOS:000441874400004 |
内容类型 | 期刊论文 |
源URL | [http://210.75.237.14/handle/351003/30610] |
专题 | 国家天然药物工程技术研究中心_天然产物研究 |
作者单位 | 1.Univ Chinese Acad Sci, Beijing, Peoples R China 2.Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu, Sichuan, Peoples R China; |
推荐引用方式 GB/T 7714 | Zhang, Xiaoke,Pan, Yang,Liang, Peng,et al. Oxadiazepine Synthesis by Formal [4+3] Cycloaddition of o-Chloromethyl Arylsulfonamides with Nitrones Promoted by NaHCO3[J]. ADVANCED SYNTHESIS & CATALYSIS,2018,360(16):3015-3019. |
APA | Zhang, Xiaoke.,Pan, Yang.,Liang, Peng.,Pang, Lu.,Ma, Xiaofeng.,...&Shao, Huawu.(2018).Oxadiazepine Synthesis by Formal [4+3] Cycloaddition of o-Chloromethyl Arylsulfonamides with Nitrones Promoted by NaHCO3.ADVANCED SYNTHESIS & CATALYSIS,360(16),3015-3019. |
MLA | Zhang, Xiaoke,et al."Oxadiazepine Synthesis by Formal [4+3] Cycloaddition of o-Chloromethyl Arylsulfonamides with Nitrones Promoted by NaHCO3".ADVANCED SYNTHESIS & CATALYSIS 360.16(2018):3015-3019. |
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