Phenalenyl-Based Photocatalyst for Bioinspired Oxidative Dehydrogenation of N-Heterocycles and Benzyl Alcohols DOI
Vishali Pathania, Sudipta Raha Roy

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(6), С. 4145 - 4155

Опубликована: Фев. 28, 2024

The environmental benefits of molecular oxygen as the oxidizing agent in oxidation reactions that synthesize fine chemicals cannot be overstated. Increased interest developing robust photocatalysts is stimulated by fact current photocatalytic transformation boom has made previously inaccessible synthetic approaches possible. Motivated enzymatic catalysis, employing a reusable phenalenyl-based photocatalyst, we have successfully developed oxidative dehydrogenation utilizing greener oxidant. Under photoinduced conditions, different types saturated N-heterocycles and alcohols were dehydrogenated. versatility this bioinspired protocol demonstrated wide variety N-heteroaromatics, such quinoline, carbazole, quinoxaline, acridine, indole derivatives, well aldehydes ketones, synthesized. Detailed mechanistic studies validate proposed mechanism. Fluorescence lifetime CV experiments revealed crucial role water on efficiency reaction. present also provides chemoselectivity scalability, leading to superior results allowing for functionalization bioactive molecules at late stage sustainable manner.

Язык: Английский

Seawater electrolysis for fuels and chemicals production: fundamentals, achievements, and perspectives DOI
Lin Chen,

Chang Yu,

Junting Dong

и другие.

Chemical Society Reviews, Год журнала: 2024, Номер 53(14), С. 7455 - 7488

Опубликована: Янв. 1, 2024

Seawater electrolysis for the production of fuels and chemicals involved in onshore offshore plants powered by renewable energies offers a promising avenue unique advantages energy environmental sustainability. Nevertheless, seawater presents long-term challenges issues, such as complex composition, potential side reactions, deposition poisoning microorganisms metal ions, well corrosion, thus hindering rapid development technology. This review focuses on value-added (hydrogen beyond) fine through electrolysis, step towards sustainable carbon neutrality. The principle related are first introduced, redox reaction mechanisms summarized. Strategies operating anodes cathodes including application chloride- impurity-resistant electrocatalysts/membranes reviewed. We comprehensively summarize (hydrogen, monoxide, sulfur, ammonia,

Язык: Английский

Процитировано

28

Electroreduction of unactivated alkenes using water as hydrogen source DOI Creative Commons
Yanwei Wang, Qian Wang, Lei Wu

и другие.

Nature Communications, Год журнала: 2024, Номер 15(1)

Опубликована: Март 30, 2024

Abstract Herein, we report an electroreduction of unactivated alkyl alkenes enabled by [Fe]-H, which is provided through the combination anodic iron salts and silane generated in situ via cathodic reduction, using H 2 O as H-source. The catalytic amounts Si-additive work H-carrier from to generate a highly active species under continuous electrochemical conditions. This approach shows broad substrate scope good functional group compatibility. In addition hydrogenation, use D instead provides desired deuterated products yields with excellent D-incorporation (up >99%). Further late-stage hydrogenation complex molecules drug derivatives demonstrate potential application pharmaceutical industry. Mechanistic studies are performed provide support for proposed mechanistic pathway.

Язык: Английский

Процитировано

21

Recent Advances in Deuteration Reactions DOI
Hao Li, Shabbir Muhammad, Wu Li

и другие.

Chinese Journal of Chemistry, Год журнала: 2023, Номер 42(10), С. 1145 - 1156

Опубликована: Дек. 26, 2023

Comprehensive Summary The deuteration of organic compounds has attracted more attentions in recent years for the potential applications new drug discovery and synthetic chemistry. For this purpose, many efficient deuterium labeling methodologies have been developed, including hydrogen isotope exchange (HIE), reductive deuteration, dehalogenative that allow synthesis selectively deuterated compounds. In last few years, great breakthroughs selective achieved interest molecules is rising. review, we summarized developments since 2021. Several types key processes incorporation reactions, H/D exchange, are introduced discussed. Key Scientists 2000s, Derdau Atzrodt's group made contributions to directing assisted noble‐metal catalyzed arenes labeled During same period, Sajiki co‐workers completed a series reactions by heterogeneous platinum‐group metal catalysts. Since 2015, Gregory Pieters developed ruthenium catalysts exchange. 2016, Chirik's presence homogeneous iron complex. David MacMillan coworkers photocatalyzed HIE α‐amino C(sp 3 )–H bonds. From 2020, nanoelectrodes were designed deuterations unactivated unsaturated bonds Zhang's group. Recently, Beller's several strategies isotopic using earth‐abundant Our review latest important

Язык: Английский

Процитировано

28

Electrochemical NiH‐Catalyzed C(sp3)−C(sp3) Coupling of Alkyl Halides and Alkyl Alkenes DOI Open Access
Pengfei Li,

Guangsheng Kou,

Tian Feng

и другие.

Angewandte Chemie International Edition, Год журнала: 2023, Номер 62(44)

Опубликована: Сен. 14, 2023

Herein, an electrochemically driven NiH-catalyzed reductive coupling of alkyl halides and alkenes for the construction Csp3 -Csp3 bonds is firstly reported. Notably, serve dual function as substrates hydrogen sources to generate NiH species under electrochemical conditions. The tunable nature this reaction realized by introducing intramolecular coordinating group substrate, where product can be easily adjusted give desired branched products. method proceeds mild conditions, exhibits a broad substrate scope, affords moderate excellent yields with over 70 examples, including late-stage modification natural products drug derivatives. Mechanistic insights offer evidence process. sp3 -carbon-halogen activated through single electron transfer (SET) nickel catalyst in its low valence state, generated cathodic reduction, generation from pivotal transformation.

Язык: Английский

Процитировано

24

Electrochemical C−H deuteration of pyridine derivatives with D2O DOI Creative Commons
Zhiwei Zhao,

Ranran Zhang,

Yaowen Liu

и другие.

Nature Communications, Год журнала: 2024, Номер 15(1)

Опубликована: Май 7, 2024

Herein, we develop a straightforward, metal-free, and acid-/base-free electrochemical C4-selective C - H deuteration of pyridine derivatives with economic convenient D

Язык: Английский

Процитировано

14

Microenvironment regulation breaks the Faradaic efficiency-current density trade-off for electrocatalytic deuteration using D2O DOI Creative Commons
Meng He, Rui Li, Chuanqi Cheng

и другие.

Nature Communications, Год журнала: 2024, Номер 15(1)

Опубликована: Июнь 19, 2024

Abstract The high Faradaic efficiency (FE) of the electrocatalytic deuteration organics with D 2 O at a large current density is significant for deuterated electrosynthesis. However, FE and are two ends seesaw because severe evolution side reaction nearly industrial densities. Herein, we report combined scenario nanotip-enhanced electric field surfactant-modified interface microenvironment to enable arylacetonitrile in an 80% −100 mA cm −2 . increased concentration low activation energy due along tips accelerated transfer suppressed by surfactant-created deuterophobic contribute breaking trade-off between density. Furthermore, application our strategy other reactions improved efficiencies rationalizes design concept.

Язык: Английский

Процитировано

13

Transition-metal-, oxidant- and additive-free multi-component synthesis of alkyl heteroaryl BCPs enabled by visible-light-induced phosphine-catalyzed halogen-atom transfer DOI
Jun Xu,

Yu Hong,

Ruiyuan Xu

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер unknown

Опубликована: Янв. 1, 2024

This study describes a pioneering visible-light-induced phosphine-catalyzed halogen-atom transfer (XAT) strategy that heralds new era in the difunctionalization of [1.1.1]propellane.

Язык: Английский

Процитировано

12

Photoelectrochemical nickel-catalyzed carboacylation/silanoylation of alkenes with unactivated C/Si–H bonds DOI
Lanfen Wang,

Xiangyu Huo,

Xiao‐Zhi He

и другие.

Green Chemistry, Год журнала: 2024, Номер 26(14), С. 8315 - 8322

Опубликована: Янв. 1, 2024

A photoelectrochemical approach for the carboacylation/silanoylation of alkenes with alkanes/hydrosilanes is described. The method offers a new perspective chemists to rapidly obtain various ketones high levels structural complexity.

Язык: Английский

Процитировано

10

Electrochemical Nickel‐Catalyzed Hydrogenation DOI
Liubo Li, Xinyi Wang, Niankai Fu

и другие.

Angewandte Chemie International Edition, Год журнала: 2024, Номер 63(22)

Опубликована: Март 20, 2024

Olefin hydrogenation is one of the most important transformations in organic synthesis. Electrochemical transition metal-catalyzed an attractive approach to replace dangerous hydrogen gas with electrons and protons. However, this reaction poses major challenges due rapid evolution (HER) metal-hydride species that outcompetes alkene step, facile deposition metal catalyst at electrode stalls reaction. Here we report economical efficient strategy achieve high selectivity for reactivity over well-established HER. Using inexpensive bench-stable nickel salt as catalyst, mild features outstanding substrate generality functional group compatibility, distinct chemoselectivity. In addition, hydrodebromination alkyl aryl bromides could be realized using same system a different ligand, chemoselectivity between achieved through ligand selection. The practicability our method has been demonstrated by success large-scale synthesis catalytic amount electrolyte minimal solvent. Cyclic voltammetry kinetic studies were performed, which support Ni

Язык: Английский

Процитировано

10

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

8