• 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

胺的C-H键官能团化:多种方法的图形概述

C-H Bond Functionalization of Amines: A Graphical Overview of Diverse Methods.

作者信息

Dutta Subhradeep, Li Bowen, Rickertsen Dillon R L, Valles Daniel A, Seidel Daniel

机构信息

Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, FL 32611, USA.

出版信息

SynOpen. 2021;5(3):173-228. doi: 10.1055/s-0040-1706051. Epub 2021 Aug 12.

DOI:10.1055/s-0040-1706051
PMID:34825124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8612105/
Abstract

This Graphical Review provides a concise overview of the manifold and mechanistically diverse methods that enable the functionalization of sp C-H bonds in amines and their derivatives.

摘要

本图形综述简要概述了多种方法及其不同的作用机制,这些方法能够实现胺类及其衍生物中sp C-H键的官能化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/bdf6db9450cb/nihms-1755674-f0053.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/39bbfcd6331a/nihms-1755674-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/4ef194f2cf56/nihms-1755674-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/c2b852a34f11/nihms-1755674-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/2ca377ff0646/nihms-1755674-f0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/01564d2b201f/nihms-1755674-f0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/80c2917ad35c/nihms-1755674-f0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/2ac849ab635a/nihms-1755674-f0013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/9a70aadbe387/nihms-1755674-f0014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/10ddf32387f5/nihms-1755674-f0015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/2492af92fcca/nihms-1755674-f0016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/b8d58f34cdf3/nihms-1755674-f0017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/3feb7722a443/nihms-1755674-f0018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/7565e4434a2d/nihms-1755674-f0019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/782ff265abe7/nihms-1755674-f0020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/3acc61a2f77c/nihms-1755674-f0021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/c85bb8172a1d/nihms-1755674-f0022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/8799465fcb1e/nihms-1755674-f0023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/6a97509f04fa/nihms-1755674-f0024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/6b7fe1cc120d/nihms-1755674-f0025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/f84aeb67428a/nihms-1755674-f0026.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/c7b648166db4/nihms-1755674-f0027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/b47fc8344b62/nihms-1755674-f0028.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/d33d304bb0a6/nihms-1755674-f0029.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/99c598374626/nihms-1755674-f0030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/ccb4262675ca/nihms-1755674-f0031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/79f36df8bafc/nihms-1755674-f0032.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/120bad0c8700/nihms-1755674-f0033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/2cb7851ee281/nihms-1755674-f0034.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/d5f344f2dc69/nihms-1755674-f0035.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/61932304c747/nihms-1755674-f0036.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/8bab13346a29/nihms-1755674-f0037.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/f16920b3b23c/nihms-1755674-f0038.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/92f918e7ce9c/nihms-1755674-f0039.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/4971c9f14621/nihms-1755674-f0040.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/6d021ca357b4/nihms-1755674-f0041.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/5c9ed7a4f930/nihms-1755674-f0042.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/812e15e44f57/nihms-1755674-f0043.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/633fae327174/nihms-1755674-f0044.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/c7cc33fed67c/nihms-1755674-f0045.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/2b37eff6efcf/nihms-1755674-f0046.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/b80677f2dd84/nihms-1755674-f0047.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/3f694fe70484/nihms-1755674-f0048.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/ff605faae84b/nihms-1755674-f0049.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/574143b72de2/nihms-1755674-f0050.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/dac393ce2585/nihms-1755674-f0051.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/20ab34b7ffd1/nihms-1755674-f0052.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/bdf6db9450cb/nihms-1755674-f0053.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/39bbfcd6331a/nihms-1755674-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/4ef194f2cf56/nihms-1755674-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/c2b852a34f11/nihms-1755674-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/2ca377ff0646/nihms-1755674-f0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/01564d2b201f/nihms-1755674-f0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/80c2917ad35c/nihms-1755674-f0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/2ac849ab635a/nihms-1755674-f0013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/9a70aadbe387/nihms-1755674-f0014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/10ddf32387f5/nihms-1755674-f0015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/2492af92fcca/nihms-1755674-f0016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/b8d58f34cdf3/nihms-1755674-f0017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/3feb7722a443/nihms-1755674-f0018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/7565e4434a2d/nihms-1755674-f0019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/782ff265abe7/nihms-1755674-f0020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/3acc61a2f77c/nihms-1755674-f0021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/c85bb8172a1d/nihms-1755674-f0022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/8799465fcb1e/nihms-1755674-f0023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/6a97509f04fa/nihms-1755674-f0024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/6b7fe1cc120d/nihms-1755674-f0025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/f84aeb67428a/nihms-1755674-f0026.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/c7b648166db4/nihms-1755674-f0027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/b47fc8344b62/nihms-1755674-f0028.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/d33d304bb0a6/nihms-1755674-f0029.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/99c598374626/nihms-1755674-f0030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/ccb4262675ca/nihms-1755674-f0031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/79f36df8bafc/nihms-1755674-f0032.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/120bad0c8700/nihms-1755674-f0033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/2cb7851ee281/nihms-1755674-f0034.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/d5f344f2dc69/nihms-1755674-f0035.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/61932304c747/nihms-1755674-f0036.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/8bab13346a29/nihms-1755674-f0037.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/f16920b3b23c/nihms-1755674-f0038.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/92f918e7ce9c/nihms-1755674-f0039.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/4971c9f14621/nihms-1755674-f0040.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/6d021ca357b4/nihms-1755674-f0041.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/5c9ed7a4f930/nihms-1755674-f0042.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/812e15e44f57/nihms-1755674-f0043.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/633fae327174/nihms-1755674-f0044.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/c7cc33fed67c/nihms-1755674-f0045.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/2b37eff6efcf/nihms-1755674-f0046.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/b80677f2dd84/nihms-1755674-f0047.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/3f694fe70484/nihms-1755674-f0048.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/ff605faae84b/nihms-1755674-f0049.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/574143b72de2/nihms-1755674-f0050.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/dac393ce2585/nihms-1755674-f0051.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/20ab34b7ffd1/nihms-1755674-f0052.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18a/8612105/bdf6db9450cb/nihms-1755674-f0053.jpg

相似文献

1
C-H Bond Functionalization of Amines: A Graphical Overview of Diverse Methods.胺的C-H键官能团化:多种方法的图形概述
SynOpen. 2021;5(3):173-228. doi: 10.1055/s-0040-1706051. Epub 2021 Aug 12.
2
Iridium-Catalyzed, β-Selective C(sp)-H Silylation of Aliphatic Amines To Form Silapyrrolidines and 1,2-Amino Alcohols.铱催化的、β-选择性的 C(sp3)-H 硅烷化反应在脂肪族伯胺中形成硅氮杂吡咯烷和 1,2-氨基醇。
J Am Chem Soc. 2018 Dec 26;140(51):18032-18038. doi: 10.1021/jacs.8b10428. Epub 2018 Dec 13.
3
Palladium(0)-Catalyzed Benzylic C(sp)-H Functionalization for the Concise Synthesis of Heterocycles and Its Applications.钯(0)催化的苄基C(sp)-H官能团化用于杂环的简洁合成及其应用
Chem Pharm Bull (Tokyo). 2017;65(5):409-425. doi: 10.1248/cpb.c16-00969.
4
N-Heterocyclic Carbene Enabled Functionalization of Inert C(Sp)-H Bonds via Hydrogen Atom Transfer (HAT) Processes.通过氢原子转移(HAT)过程实现的N-杂环卡宾介导的惰性C(Sp)-H键官能化。
Chemistry. 2024 Aug 22;30(47):e202401811. doi: 10.1002/chem.202401811. Epub 2024 Aug 2.
5
Enantioselective Single and Dual α-C-H Bond Functionalization of Cyclic Amines via Enzymatic Carbene Transfer.通过酶催化卡宾转移实现环状胺的对映选择性单和双 α-C-H 键官能化。
J Am Chem Soc. 2023 Jan 11;145(1):537-550. doi: 10.1021/jacs.2c10775. Epub 2022 Dec 21.
6
Hydride-Abstraction-Initiated Catalytic Stereoselective Intermolecular Bond-Forming Processes.氢化物消除引发的催化立体选择性分子间成键过程。
Acc Chem Res. 2022 Dec 6;55(23):3537-3550. doi: 10.1021/acs.accounts.2c00638. Epub 2022 Nov 17.
7
Steric, Electronic and Conformational Synergistic Effects in the Gold(I)-catalyzed α-C-H Bond Functionalization of Tertiary Amines.金(I)催化叔胺α-C-H键官能团化反应中的空间、电子和构象协同效应
Angew Chem Int Ed Engl. 2023 Jan 16;62(3):e202212893. doi: 10.1002/anie.202212893. Epub 2022 Oct 18.
8
Condensation-Based Methods for the C-H Bond Functionalization of Amines.基于缩合反应的胺类C-H键官能团化方法
Synthesis (Stuttg). 2021 Nov;53(21):3869-3908. doi: 10.1055/a-1631-2140. Epub 2021 Sep 2.
9
Copper-catalyzed aerobic oxidative C-H functionalization of substituted pyridines: synthesis of imidazopyridine derivatives.铜催化取代吡啶的有氧氧化 C-H 官能化反应:咪唑并吡啶衍生物的合成。
Chemistry. 2013 Dec 2;19(49):16804-8. doi: 10.1002/chem.201302737. Epub 2013 Oct 21.
10
Photoredox-catalyzed C()─H radical functionalization to enable asymmetric synthesis of α-chiral alkyl phosphine.光氧化还原催化的C()─H自由基官能团化用于实现α-手性烷基膦的不对称合成。 (注:原文中C()表述有误,推测可能是C-H,翻译按此推测进行)
Sci Adv. 2024 Jun 7;10(23):eadn9738. doi: 10.1126/sciadv.adn9738. Epub 2024 Jun 5.

引用本文的文献

1
Selective -Cyclic α-Functionalization of Saturated -Alkyl Piperidines.饱和烷基哌啶的选择性 - 环α-官能化
J Org Chem. 2025 Aug 29;90(34):12226-12239. doi: 10.1021/acs.joc.5c01742. Epub 2025 Aug 18.
2
Regiodivergent α- and β-Functionalization of Saturated -Heterocycles by Photocatalytic Oxidation.光催化氧化实现饱和杂环的区域发散性α-和β-官能化
J Am Chem Soc. 2025 Jul 9;147(27):23381-23386. doi: 10.1021/jacs.5c06177. Epub 2025 Jun 30.
3
Dual relay Rh-/Pd-catalysis enables β-C(sp)-H arylation of α-substituted amines.

本文引用的文献

1
-Functionalization of Saturated Aza-Heterocycles Enabled by Organic Photoredox Catalysis.- 有机光氧化还原催化实现的饱和氮杂环的功能化
ACS Catal. 2021 Mar 5;11(5):3153-3158. doi: 10.1021/acscatal.1c00099. Epub 2021 Feb 24.
2
Traceless Redox-Annulations of Alicyclic Amines.脂环胺的无痕氧化还原环化反应
SynOpen. 2020;4(4):123-131. doi: 10.1055/s-0040-1706004. Epub 2020 Dec 16.
3
Synthesis of -aryl amines enabled by photocatalytic dehydrogenation.通过光催化脱氢实现的-芳基胺的合成。
双接力铑/钯催化实现了α-取代胺的β-C(sp)-H芳基化反应。
Chem Sci. 2025 Jan 28;16(9):4167-4174. doi: 10.1039/d4sc06806h. eCollection 2025 Feb 26.
4
Acridine/Lewis Acid Complexes as Powerful Photocatalysts: A Combined Experimental and Mechanistic Study.吖啶/路易斯酸配合物作为高效光催化剂:实验与机理的联合研究
ACS Catal. 2024 Oct 4;14(19):14574-14585. doi: 10.1021/acscatal.4c04897. Epub 2024 Sep 16.
5
Photocatalytic Decarboxylative Alkylation of Cyclic Imine-BF Complexes: A Modular Route to Functionalized Azacycles.环状亚胺 - BF 配合物的光催化脱羧烷基化反应:一种合成功能化氮杂环的模块化方法。
J Am Chem Soc. 2024 Sep 25;146(38):26331-26339. doi: 10.1021/jacs.4c08754. Epub 2024 Sep 12.
6
Regioselective α-Phosphonylation of Unprotected Alicyclic Amines.未保护的脂环胺的区域选择性α-膦酰化反应
Org Lett. 2024 Jul 19;26(28):5972-5977. doi: 10.1021/acs.orglett.4c02037. Epub 2024 Jul 5.
7
Electrochemical synthesis of peptide aldehydes via C‒N bond cleavage of cyclic amines.通过环状胺的 C‒N 键断裂电化学合成肽醛。
Nat Commun. 2024 Jun 18;15(1):5181. doi: 10.1038/s41467-024-49223-y.
8
C(sp)-H cyclizations of 2-(2-vinyl)phenoxy--anilines.2-(2-乙烯基)苯氧基苯胺的C(sp) -H环化反应
RSC Adv. 2024 May 23;14(24):16784-16800. doi: 10.1039/d3ra08974f. eCollection 2024 May 22.
9
Copper-Nitroxyl-Catalyzed α-Oxygenation of Cyclic Secondary Amines Including Application to Late-Stage Functionalization.铜-氮氧自由基催化的环状仲胺的α-氧官能团化反应,包括在后期官能团化中的应用。
J Am Chem Soc. 2024 May 29;146(21):14439-14444. doi: 10.1021/jacs.4c04359. Epub 2024 May 14.
10
Redox-neutral α-functionalization of pyrrolidines: facile access to α-aryl-substituted pyrrolidines.吡咯烷的氧化还原中性α-官能团化:简便合成α-芳基取代吡咯烷的方法。
RSC Adv. 2024 Apr 15;14(17):11986-11991. doi: 10.1039/d4ra00983e. eCollection 2024 Apr 10.
Chem Sci. 2020 Dec 8;12(5):1915-1923. doi: 10.1039/d0sc04890a.
4
C-H functionalization reactions enabled by hydrogen atom transfer to carbon-centered radicals.通过氢原子转移到碳中心自由基实现的C-H官能团化反应。
Chem Sci. 2020 Nov 16;11(48):12974-12993. doi: 10.1039/d0sc04881j.
5
Iron-catalyzed α-C-H functionalization of π-bonds: cross-dehydrogenative coupling and mechanistic insights.铁催化的π键α-C-H官能团化:交叉脱氢偶联及机理研究
Chem Sci. 2020 Oct 16;11(45):12316-12322. doi: 10.1039/d0sc05091a.
6
Sulfamides direct radical-mediated chlorination of aliphatic C-H bonds.磺胺类化合物可直接实现自由基介导的脂肪族碳氢键氯化反应。
Chem Sci. 2019 Nov 8;11(1):217-223. doi: 10.1039/c9sc03428e.
7
α-C-H/N-H Annulation of Alicyclic Amines via Transient Imines: Preparation of Polycyclic Lactams.α-C-H/N-H 环化芳胺反应:通过瞬态亚胺制备多环内酰胺。
Org Lett. 2021 May 7;23(9):3729-3734. doi: 10.1021/acs.orglett.1c01125. Epub 2021 Apr 21.
8
Palladium-Mediated C -H Functionalization of Alicyclic Amines.钯介导的环状胺的 C-H 官能化反应。
Angew Chem Int Ed Engl. 2021 May 10;60(20):11227-11230. doi: 10.1002/anie.202101782. Epub 2021 Apr 8.
9
Key Mechanistic Features of the Silver(I)-Mediated Deconstructive Fluorination of Cyclic Amines: Multistate Reactivity versus Single-Electron Transfer.银(I)介导的环状胺解构氟化反应的关键机制特征:多态反应与单电子转移。
J Am Chem Soc. 2021 Mar 17;143(10):3889-3900. doi: 10.1021/jacs.0c13061. Epub 2021 Mar 3.
10
C-H Activation: Toward Sustainability and Applications.碳-氢活化:迈向可持续发展与应用
ACS Cent Sci. 2021 Feb 24;7(2):245-261. doi: 10.1021/acscentsci.0c01413. Epub 2021 Feb 2.