Oxidants Controlled C−H Bond Functionalization of N‐Aryltetrahydroisoquinolines: The Construction of the Quaternary Carbon Center and Cleavage of the C−N Bond DOI
Yuqin Chen, Shuwei Zhang,

Tong Li

и другие.

Chemistry - A European Journal, Год журнала: 2023, Номер 30(3)

Опубликована: Окт. 25, 2023

Initiated by triarylamine radical cation salt (TBPA), the direct C-H bond functionalization of α-N-aryltetrahydroisoquinoline esters was smoothly realized, giving a series α-hydroxylated derivatives with quaternary carbon center in good yields. Differently, presence tert-butyl nitrite (TBN), C-N single cleaved to keto esters. The mechanistic study revealed that these reactions were mediated similar mechanism, which N-nitrosation might provide driving force cleavage.

Язык: Английский

Electrochemical Promoted Three-Component Trifluoromethylation/Spirocyclization Reaction of N-Arylsulfonylacrylamides to 4-Azaspiro[4.5]decanes DOI

Zhi-Long Lei,

Tai-Chen Liu,

Fei‐Hu Cui

и другие.

Organic Letters, Год журнала: 2023, Номер 25(32), С. 6001 - 6005

Опубликована: Авг. 7, 2023

An electrochemical facilitated three-component trifluoromethylation/spirocyclization reaction of N-(arylsulfonyl)acrylamides, CF3SO2Na, and H2O has been developed. Without the requirement chemical oxidants, a number unexplored trifluoromethylated 4-azaspiro[4.5]decanes were obtained in satisfactory yields under mild conditions. This work provides new synthetic strategy for fluorine-containing spirocyclic compounds shows perspective reactivity study N-(arylsulfonyl)acrylamides.

Язык: Английский

Процитировано

11

Designing a Chiral Electrode for Enantioselective Electro-organic Cyanation of Styrene Utilizing Copper Nanoparticles on Graphene Oxide Modified with L-Alanine in Deep Eutectic Solvent and Electrolyte Environment DOI
Muath Jabbar Tarfa Al-Abbasee,

Shakir Mahmood Saeed,

Zaman Abdalhussein Ibadi Alaridhee

и другие.

Journal of Molecular Structure, Год журнала: 2025, Номер unknown, С. 141303 - 141303

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Recent advances in electrochemical copper catalysis for modern organic synthesis DOI Creative Commons

Y-H. Kim,

Won Jun Jang

Beilstein Journal of Organic Chemistry, Год журнала: 2025, Номер 21, С. 155 - 178

Опубликована: Янв. 16, 2025

In recent decades, organic electrosynthesis has emerged as a practical, sustainable, and efficient approach that facilitates valuable transformations in synthetic chemistry. Combining electrochemistry with transition-metal catalysis is promising rapidly growing methodology for effectively forming challenging C-C C-heteroatom bonds complex molecules sustainable manner. this review, we summarize the advances combination of copper various transformations.

Язык: Английский

Процитировано

0

α-Thiocyanation of Enol Acetates and Sodium Thiocyanate under Electrochemical Conditions DOI
Jinpeng Zhang, Yuliang Qian, Man Ning

и другие.

Chinese Journal of Organic Chemistry, Год журнала: 2025, Номер 45(1), С. 189 - 189

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Advances in Asymmetric Electrochemical Synthesis DOI

Chun Gao,

Xin Liu, Minghui Wang

и другие.

Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(3), С. 673 - 673

Опубликована: Янв. 1, 2024

Язык: Английский

Процитировано

3

When transition-metal catalysis meets electrosynthesis: a recent update DOI
Fei Lian, Jiuling Li, Kun Xu

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(22), С. 4390 - 4419

Опубликована: Янв. 1, 2024

The merger of organic electrosynthesis with 3d transition-metal catalysis has offered huge opportunities for modern synthesis. This review summarizes the key advancements in this direction published recent two years.

Язык: Английский

Процитировано

3

Metal-ligand cooperativity in chemical electrosynthesis DOI Creative Commons
Maia E. Czaikowski,

Sophie W. Anferov,

John S. Anderson

и другие.

Chem Catalysis, Год журнала: 2024, Номер 4(3), С. 100922 - 100922

Опубликована: Фев. 19, 2024

Язык: Английский

Процитировано

2

Synthesis of N,N‐Disubstituted Hydrazines by Electrocatalytic Addition of Hydrazines to α,β‐Unsaturated Carbonyl Compounds DOI

Qingyu Xu,

Chengwei Zhang, Hang Xu

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2024, Номер 366(12), С. 2829 - 2834

Опубликована: Апрель 24, 2024

Abstract A strategy for the synthesis of N,N ‐disubstituted hydrazines via electrocatalytic addition hydrazine to α,β‐unsaturated carbonyl compounds is reported. The reaction was carried out under constant current electrolytic conditions in an undivided cell. Using this methodology, various were prepared 57–94% yield 40 minutes. By adding cyclohexanone and acetic acid mixture heating 2 hours, a one‐pot N ‐substituted indoles also developed. Furthermore, based on cyclic voltammetry control experiments, plausible mechanism involving radical pathway proposed.

Язык: Английский

Процитировано

2

Synthesis and characterization of fullerene modified with copper nanoparticles catalyzed C H bond activation as a sustainable and green catalyst for electro synthesis of benzothiazole derivatives DOI
Sherzod Abdullaev, Mosleh M. Abomughaid, Dheyaa J. Jasim

и другие.

Journal of Molecular Structure, Год журнала: 2023, Номер 1302, С. 137413 - 137413

Опубликована: Дек. 24, 2023

Язык: Английский

Процитировано

6

Electrochemically‐Driven Organocatalytic Enantioselective Oxidative Coupling of Tetrahydroisoquinolines and Acrylaldehyde DOI Open Access

Qiying Zhang,

Luxin Li, Songlin Wang

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2023, Номер 365(20), С. 3455 - 3460

Опубликована: Авг. 24, 2023

Abstract An electrochemically‐driven organocatalytic enantioselective oxidative coupling of tetrahydroisoquinolines and acrylaldehyde was developed. Various chiral C1‐alkenyl derivatives were obtained with 69–86% yields 93:7–96:4 er. Notable features this reaction include asymmetric organocatalysis (5.0 mol% β‐ICD as catalyst), electricity the oxidant, air atmosphere, undivided cell. This synthetic route offers access to various optically active C1‐substituted derivatives.

Язык: Английский

Процитировано

4