Electroreductive Radical Addition–Polar Cyclization Cascade to Access Cycloalkanes DOI
Yi Wang,

Jiachen Deng,

Andrew J. Ressler

и другие.

Organic Letters, Год журнала: 2023, Номер unknown

Опубликована: Дек. 29, 2023

Compared with flat aromatic scaffolds, three-dimensional aliphatic ring systems feature high structural complexity and topological diversity and, thus, have received increasing attention in drug discovery. Herein, we describe a mild general electrochemical method for the modular synthesis of structurally distinct cyclic compounds, including monocyclic alkanes, benzo-fused systems, spirocycles, from readily available alkenes alkyl halides via radical–polar crossover mechanism.

Язык: Английский

A tutorial on asymmetric electrocatalysis DOI
Jonas Rein, Samson B. Zacate, Kaining Mao

и другие.

Chemical Society Reviews, Год журнала: 2023, Номер 52(23), С. 8106 - 8125

Опубликована: Янв. 1, 2023

This tutorial review delves into the unique advantages of electrochemistry in context asymmetric catalysis, first providing a brief introduction to electrosynthesis, then exploring representative case studies with mechanistic focus.

Язык: Английский

Процитировано

65

Electrochemical radical-polar crossover: a radical approach to polar chemistry DOI

Zhoumei Tan,

Haonan Zhang, Kun Xu

и другие.

Science China Chemistry, Год журнала: 2023, Номер 67(2), С. 450 - 470

Опубликована: Ноя. 3, 2023

Язык: Английский

Процитировано

51

Three-Component Cross-Electrophile Coupling: Regioselective Electrochemical Dialkylation of Alkenes DOI
Lingxiang Lu, Yi Wang,

Wendy Zhang

и другие.

Journal of the American Chemical Society, Год журнала: 2023, Номер 145(41), С. 22298 - 22304

Опубликована: Окт. 6, 2023

The cross-electrophile dialkylation of alkenes enables the formation two C(sp

Язык: Английский

Процитировано

35

Electrochemically Driven Deoxygenative Borylation of Alcohols and Carbonyl Compounds DOI
Weiyang Guan,

Yejin Chang,

Song Lin

и другие.

Journal of the American Chemical Society, Год журнала: 2023, Номер 145(31), С. 16966 - 16972

Опубликована: Июль 27, 2023

We present a new, unified approach for the transformation of benzylic and allylic alcohols, aldehydes, ketones into boronic esters under electroreductive conditions. Key to our strategy is use readily available pinacolborane, which serves both as an activator electrophile by first generating redox-active trialkylborate species then delivering desired deoxygenatively borylated product. This applicable variety substrates can be employed late-stage functionalization complex molecules.

Язык: Английский

Процитировано

29

The role of silicon in drug discovery: a review DOI Creative Commons
Jenny‐Lee Panayides, Darren L. Riley, Felix Hasenmaile

и другие.

RSC Medicinal Chemistry, Год журнала: 2024, Номер 15(10), С. 3286 - 3344

Опубликована: Янв. 1, 2024

This review aims to highlight the role of silicon in drug discovery.

Язык: Английский

Процитировано

13

Electroreductive Arylcarboxylation of Styrenes with CO2 and Aryl Halides via a Radical–Polar Crossover Mechanism DOI

Fenfen Xie,

Fen Han,

Qian Su

и другие.

Organic Letters, Год журнала: 2024, Номер 26(21), С. 4427 - 4432

Опубликована: Май 17, 2024

2,3-Diaryl propanoic acids are important structures as a result of their widespread presence in numerous bioactive compounds. However, the limitations existing synthetic techniques include requirement for costly catalysts and limited substrates. Here, we developed novel electroreductive arylcarboxylation alkenes with CO2 based on radical–polar crossover pathway assisted by easily accessible dimethyl terephthalate reductive mediator. This method will provide an efficient strategy synthesis 2,3-diarylpropanoic acids.

Язык: Английский

Процитировано

10

Allylgermane synthesis via facile and general nickela-electrocatalyzed electrophile coupling DOI
Haifeng Chen,

Cai Zhai,

Chen Zhu

и другие.

Chem Catalysis, Год журнала: 2025, Номер unknown, С. 101257 - 101257

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

2

Synthesis of Alkynylsilanes: A Review of the State of the Art DOI
Krzysztof Kuciński

Advanced Synthesis & Catalysis, Год журнала: 2024, Номер 366(11), С. 2382 - 2431

Опубликована: Апрель 12, 2024

Abstract This contribution offers a comprehensive overview of methods for forging sp C−Si bonds. Over time, alkynylsilanes (silylacetylenes), once considered mere byproducts hydrosilylation processes, have become essential building blocks in organic synthesis. literature review traces the evolution their synthesis, from traditional methodologies relying on organolithium and organomagnesium compounds to more advanced cross‐coupling reactions involving hydro‐ carbosilanes. Focused primarily past 25 years (2000–2024), it also extensively references significant historical breakthroughs. By analyzing synthetic methodologies, not only survey current state knowledge but identifies areas improvement. Furthermore, emphasize importance 1‐alkynylsilanes (1‐silyl‐1‐alkynes), selected applications these are highlighted, confirming potential

Язык: Английский

Процитировано

6

A guide to troubleshooting metal sacrificial anodes for organic electrosynthesis DOI Creative Commons
Skyler D. Ware,

Wendy Zhang,

Weiyang Guan

и другие.

Chemical Science, Год журнала: 2024, Номер 15(16), С. 5814 - 5831

Опубликована: Янв. 1, 2024

Sacrificial anodes enable reductive electrosynthesis but can inadvertently limit the conditions compatible with organic reactions. Addressing challenges that arise at sacrificial improve yields and streamline reaction optimization.

Язык: Английский

Процитировано

5

Electrochemically promoted C(sp3)–C(sp2) bond formation via radical/radical anion cross-coupling DOI

Mingchun Wang,

Ao Song,

Xiupeng Wang

и другие.

Molecular Catalysis, Год журнала: 2024, Номер 562, С. 114228 - 114228

Опубликована: Май 21, 2024

Язык: Английский

Процитировано

5