题名 | Organocatalytic enantioselective [2 + 4]-annulation of γ-substituted allenoates withN-acyldiazenes for the synthesis of optically active 1,3,4-oxadiazines |
作者 | |
通讯作者 | Li,Xuechen; Li,Pengfei |
发表日期 | 2021-02-28
|
DOI | |
发表期刊 | |
ISSN | 1477-0520
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EISSN | 1477-0539
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卷号 | 19期号:8页码:1727-1731 |
摘要 | An enantioselective [2 + 4]-annulation of γ-substituted allenoates withN-acyldiazenes has been developed for the first time. In the presence of anl-proline-derived DMAP analogue, the annulation proceeded smoothly to afford a broad range of 1,3,4-oxadiazine derivatives in good to excellent yields with high stereoselectivities.;An enantioselective [2 + 4]-annulation of γ-substituted allenoates withN-acyldiazenes has been developed for the first time. In the presence of anl-proline-derived DMAP analogue, the annulation proceeded smoothly to afford a broad range of 1,3,4-oxadiazine derivatives in good to excellent yields with high stereoselectivities.;An enantioselective [2 + 4]-annulation of γ-substituted allenoates withN-acyldiazenes has been developed for the first time. In the presence of anl-proline-derived DMAP analogue, the annulation proceeded smoothly to afford a broad range of 1,3,4-oxadiazine derivatives in good to excellent yields with high stereoselectivities. |
相关链接 | [Scopus记录] |
收录类别 | |
语种 | 英语
|
学校署名 | 第一
; 通讯
|
资助项目 | National Natural Science Foundation of China[21871128]
; Guangdong Provincial Key Laboratory of Catalysis[2020B121201002]
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WOS研究方向 | Chemistry
|
WOS类目 | Chemistry, Organic
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WOS记录号 | WOS:000625235100004
|
出版者 | |
EI入藏号 | 20211010049918
|
EI主题词 | Chemistry
; Positive ions
|
EI分类号 | Chemistry:801
; Physical Chemistry:801.4
|
ESI学科分类 | CHEMISTRY
|
Scopus记录号 | 2-s2.0-85102064377
|
来源库 | Scopus
|
引用统计 |
被引频次[WOS]:12
|
成果类型 | 期刊论文 |
条目标识符 | http://sustech.caswiz.com/handle/2SGJ60CL/221613 |
专题 | 理学院_化学系 理学院 深圳格拉布斯研究院 |
作者单位 | 1.Shenzhen Grubbs Institute and Department of Chemistry,Guangdong Provincial Key Laboratory of Catalysis,College of Science,Southern University of Science and Technology,Shenzhen,518055,China 2.Department of Chemistry,State Key Lab of Synthetic Chemistry,University of Hong Kong,Hong Kong |
第一作者单位 | 化学系; 深圳格拉布斯研究院; 理学院 |
通讯作者单位 | 化学系; 深圳格拉布斯研究院; 理学院 |
第一作者的第一单位 | 化学系; 深圳格拉布斯研究院; 理学院 |
推荐引用方式 GB/T 7714 |
Guo,Xing,Chen,Xuling,Cheng,Yuyu,et al. Organocatalytic enantioselective [2 + 4]-annulation of γ-substituted allenoates withN-acyldiazenes for the synthesis of optically active 1,3,4-oxadiazines[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2021,19(8):1727-1731.
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APA |
Guo,Xing,Chen,Xuling,Cheng,Yuyu,Chang,Xiaoyong,Li,Xuechen,&Li,Pengfei.(2021).Organocatalytic enantioselective [2 + 4]-annulation of γ-substituted allenoates withN-acyldiazenes for the synthesis of optically active 1,3,4-oxadiazines.ORGANIC & BIOMOLECULAR CHEMISTRY,19(8),1727-1731.
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MLA |
Guo,Xing,et al."Organocatalytic enantioselective [2 + 4]-annulation of γ-substituted allenoates withN-acyldiazenes for the synthesis of optically active 1,3,4-oxadiazines".ORGANIC & BIOMOLECULAR CHEMISTRY 19.8(2021):1727-1731.
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条目包含的文件 | 条目无相关文件。 |
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