Unlocking the Potential of Deep Eutectic Solvents for C–H Activation and Cross-Coupling Reactions: A Review DOI Creative Commons
Yassine El Baraka, Ghanem Hamdoun, Nabil El Brahmi

et al.

Molecules, Journal Year: 2023, Volume and Issue: 28(12), P. 4651 - 4651

Published: June 8, 2023

Green chemistry principles have underpinned the development of deep eutectic solvents (DESs). In this brief overview, we discuss potential DESs as a greener alternative to volatile organic for cross-coupling and C–H activation reactions in chemistry. offer numerous benefits, such easy preparation, low toxicity, high biodegradability, replace compounds. The ability recover catalyst-solvent system enhances their sustainability. This review highlights recent advances challenges utilizing reaction media, well impact physicochemical properties on process. Several types are studied highlight effectiveness at promoting C–C bond formation. Aside from demonstrating success context, also discusses limitations future prospects

Language: Английский

Closed-loop cobalt recycling from spent lithium-ion batteries based on a deep eutectic solvent (DES) with easy solvent recovery DOI

Taibai Li,

Yige Xiong, Xiaohui Yan

et al.

Journal of Energy Chemistry, Journal Year: 2022, Volume and Issue: 72, P. 532 - 538

Published: May 13, 2022

Language: Английский

Citations

89

Bioinspired green deep eutectic solvents: preparation, catalytic activity, and biocompatibility DOI

Shaina Joarder,

Divyam Bansal,

Harshvardhan Meena

et al.

Journal of Molecular Liquids, Journal Year: 2023, Volume and Issue: 376, P. 121355 - 121355

Published: Feb. 7, 2023

Language: Английский

Citations

30

Radical Transformations towards the Synthesis of Quinoline: A Review DOI
Kumaraswamy Naidu Chitrala, Fazlur‐Rahman Nawaz Khan

Chemistry - An Asian Journal, Journal Year: 2020, Volume and Issue: 15(24), P. 4153 - 4167

Published: Nov. 2, 2020

Quinoline is considered one of the most ubiquitous heterocycles due to its engaging biological activities and synthetic utility over organic transformations. Over past few decades, numerous reports have been documented in synthesis quinolines. The classical methods including, Skraup, Friedlander, Doebner-von-Miller, Conrad-Limpach, Pfitzinger quinoline synthesis, so forth, these are well-known construct principal scaffold with several advantages limitations. Recently, radical insertion or catalyzed reactions emerged as a powerful efficient tool high atom efficiency step economy. In this concern, minireview mainly focused on developments via reactions. addition, brief description preparation procedure, reactivity, mechanisms also included, where possible. Respectively, quinolines classified summarized based it will help researchers grab information exploration area, Quinolines promising pharmacophores.

Language: Английский

Citations

51

Lignin-derived Zn single atom/N-codoped porous carbon for α-alkylation of aromatic ketones with alcohols via borrowing hydrogen strategy DOI
Xueping Zhang, Guoping Lu, Kun Wang

et al.

Nano Research, Journal Year: 2021, Volume and Issue: 15(3), P. 1874 - 1881

Published: Sept. 2, 2021

Language: Английский

Citations

49

Recent Advances for Alkylation of Ketones and Secondary Alcohols Using Alcohols in Homogeneous Catalysis DOI

Dongyuan Yang,

Hongli Wang, Chun‐Ran Chang

et al.

Advanced Synthesis & Catalysis, Journal Year: 2022, Volume and Issue: 364(18), P. 3100 - 3121

Published: July 4, 2022

Abstract The alkylation of ketones or secondary alcohols using as alkylating agents via hydrogen borrowing strategy presents a powerful method for the synthesis ɑ‐alkylated ketones. In this review, we summarize progress catalyzed by Ir, Pd, Rh, Ru, Mn, Fe, Co, Ni, and Cu catalysts α‐alkylation with cross‐coupling from 2017 to 2021. A wide range (aromatic aliphatic ketones) (benzylic primary alcohols, aromatic alkenyl diols) are well tolerated. Furthermore, also discuss current challenges propose perspectives on coming development in filed. objective present review is give an overview recent advances β‐alkylation alcohols. Finally, hope that will inspirations magnified image

Language: Английский

Citations

30

Dissecting the stability of Atezolizumab with renewable amino acid-based ionic liquids: Colloidal stability and anticancer activity under thermal stress DOI
Bayan Alkhawaja, Faisal Al‐Akayleh,

Zaid Al-Rubaye

et al.

International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 270, P. 132208 - 132208

Published: May 8, 2024

Language: Английский

Citations

9

Designed pincer ligand supported Co(ii)-based catalysts for dehydrogenative activation of alcohols: Studies on N-alkylation of amines, α-alkylation of ketones and synthesis of quinolines DOI
Anshu Singh, Ankur Maji, Mayank Joshi

et al.

Dalton Transactions, Journal Year: 2021, Volume and Issue: 50(24), P. 8567 - 8587

Published: Jan. 1, 2021

Base-metal Co-based catalysts Co1, Co2 and Co3 supported by pincer ligands were utilized for dehydrogenative activation of alcohols giving rise to N-alkylation amines, α-alkylation ketones synthesis quinolines.

Language: Английский

Citations

34

Copper-catalyzed dehydrogenative cyclization/alkenylation towards dihydroquinolinones DOI

K. Pari,

Nawaz Khan Fazlur-Rahman

Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: 22(20), P. 4163 - 4171

Published: Jan. 1, 2024

A mild and one-pot sequential route to access diversely substituted quinolinyl dihydroquinolinones has been proposed, using a dehydrogenative cyclization/alkenylation strategy with good yields.

Language: Английский

Citations

6

New hydrophobic deep eutectic solvent for electrochemical applications DOI Creative Commons

Nesrine Chaabene,

Kieu Ngo, Mireille Turmine

et al.

Journal of Molecular Liquids, Journal Year: 2020, Volume and Issue: 319, P. 114198 - 114198

Published: Sept. 2, 2020

Language: Английский

Citations

34

Deep Eutectic Solvents as à-la-Carte Medium for Transition-Metal-Catalyzed Organic Processes DOI Creative Commons
Xavier Marset, Gabriela Guillena

Molecules, Journal Year: 2022, Volume and Issue: 27(23), P. 8445 - 8445

Published: Dec. 2, 2022

Our society is facing a tremendous challenge to become more sustainable in every sphere of life. Regarding the chemical industry, one most significant issues be addressed use volatile organic compounds (VOCs) as solvents because they are petrol-derived and them toxic flammable. Among possible solutions, deep eutectic (DESs) have emerged alternatives VOCs catalyzed transformations other fields. The advantages these new reaction media not only related their benign physical properties and, for them, renewable sources but also due possibility being recycled after use, increasing sustainability process which involved. However, catalytic introduces challenges regarding compatibility activity known catalysts. Therefore, designed catalysts “à-la-carte” DESs systems been developed overcome this problem, maximize outcomes allow recyclability catalyst/media system. Over last decade, popularity has steadily increased, with several examples efficient metal-catalyzed transformations, showing efficiency catalysts/DES system, compared carried out VOCs. Additionally, inherent DES, unknown can using appropriated catalyst/DES All processes compiled review.

Language: Английский

Citations

20