• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

镍催化、氨基喹啉导向的未活化烯烃与有机硼酸和邻氨基苯甲酸酯的化学及区域选择性碳胺化反应

Nickel-Catalyzed, Aminoquinoline-Directed Chemo- and Regioselective Carboamination of Unactivated Olefins with Organoboronic Acids and Anthranils.

作者信息

Xie Zhongke, Cui Yushan, Xing Jiale, Gao Yang, Huo Yanping, Li Xianwei, Chen Qian

机构信息

School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China.

Jieyang Branch of Chemistry and Chemical Engineering Guangdong Laboratory, Jieyang 515200, China.

出版信息

J Org Chem. 2024 Oct 4;89(19):14151-14163. doi: 10.1021/acs.joc.4c01536. Epub 2024 Sep 19.

DOI:10.1021/acs.joc.4c01536
PMID:39298536
Abstract

A nickel-catalyzed three-component carboamination of unactivated alkenes with organoboronic acids and anthranils has been achieved for the expedient synthesis of δ-aryl and γ-amino acid derivatives. The 8-aminoquinoline (AQ) directing group is crucial for the success of the reaction, and anthranil serves as an arylnitrene precursor in this conversion. This method features mild reaction conditions, good chemo- and regioselectivity, and a broad substrate scope with good functional group tolerance.

摘要

已实现镍催化未活化烯烃与有机硼酸和邻氨基苯甲酰亚胺的三组分碳胺化反应,用于便捷合成δ-芳基和γ-氨基酸衍生物。8-氨基喹啉(AQ)导向基团对反应成功至关重要,且邻氨基苯甲酰亚胺在该转化中作为芳基氮烯前体。该方法具有反应条件温和、化学和区域选择性良好以及底物范围广且官能团耐受性好的特点。

相似文献

1
Nickel-Catalyzed, Aminoquinoline-Directed Chemo- and Regioselective Carboamination of Unactivated Olefins with Organoboronic Acids and Anthranils.镍催化、氨基喹啉导向的未活化烯烃与有机硼酸和邻氨基苯甲酸酯的化学及区域选择性碳胺化反应
J Org Chem. 2024 Oct 4;89(19):14151-14163. doi: 10.1021/acs.joc.4c01536. Epub 2024 Sep 19.
2
NiH-Catalyzed Proximal-Selective Hydroamination of Unactivated Alkenes with Anthranils.镍催化邻位选择性胺化未活化烯烃与邻苯二甲酰亚胺。
J Org Chem. 2022 Nov 4;87(21):14861-14869. doi: 10.1021/acs.joc.2c01592. Epub 2022 Oct 11.
3
Nickel-Catalyzed 8-Aminoquinoline Directed Reductive Dialkylcyclization/Homodialkylation of Unactivated Alkenes.镍催化8-氨基喹啉导向的未活化烯烃的还原二烷基环化/同二烷基化反应
Org Lett. 2023 Nov 3;25(43):7800-7804. doi: 10.1021/acs.orglett.3c02955. Epub 2023 Oct 24.
4
Directed Palladium(II)-Catalyzed Intermolecular Anti-Markovnikov Hydroarylation of Unactivated Alkenes with (Hetero)arylsilanes.钯(II)催化未活化烯烃与(杂)芳基硅烷的分子间反马氏氢芳基化反应
Org Lett. 2020 Nov 20;22(22):9022-9028. doi: 10.1021/acs.orglett.0c03416. Epub 2020 Nov 5.
5
Nickel-Catalyzed Asymmetric Reductive 1,2-Carboamination of Unactivated Alkenes.镍催化未活化烯烃的不对称还原1,2-碳胺化反应
Angew Chem Int Ed Engl. 2020 Feb 3;59(6):2328-2332. doi: 10.1002/anie.201913743. Epub 2019 Dec 27.
6
Nickel-Catalyzed Regioselective Hydroarylation of Internal Enamides.镍催化内酰胺的区域选择性氢芳基化反应
Org Lett. 2020 Dec 4;22(23):9319-9324. doi: 10.1021/acs.orglett.0c03542. Epub 2020 Nov 23.
7
Manganese-Catalyzed Hydroarylation of Unactivated Alkenes.锰催化未活化烯烃的氢芳基化反应
Angew Chem Int Ed Engl. 2020 Aug 17;59(34):14256-14260. doi: 10.1002/anie.202003830. Epub 2020 Jul 6.
8
Nickel-Catalyzed Regio- and Enantioselective Hydroamination of Unactivated Alkenes Using Carbonyl Directing Groups.镍催化的羰基导向基团促进的非活化烯烃的区域和对映选择性氢胺化反应。
J Am Chem Soc. 2022 May 25;144(20):9091-9100. doi: 10.1021/jacs.2c02343. Epub 2022 May 10.
9
Enantioselective Three-Component Fluoroalkylarylation of Unactivated Olefins through Nickel-Catalyzed Cross-Electrophile Coupling.通过镍催化的交叉电子亲核试剂偶联实现非活化烯烃的对映选择性三组分氟烷基化反应。
J Am Chem Soc. 2020 May 27;142(21):9604-9611. doi: 10.1021/jacs.0c03708. Epub 2020 May 14.
10
Cooperative Cu/azodiformate system-catalyzed allylic C-H amination of unactivated internal alkenes directed by aminoquinoline.铜/偶氮二甲酸酯协同体系催化、氨基喹啉导向的未活化内烯烃的烯丙基C-H胺化反应
Nat Commun. 2024 Feb 19;15(1):1483. doi: 10.1038/s41467-024-45875-y.