Multicomponent Reactions in Medicinal Chemistry DOI
Zefeng Wang, Alexander Dömlingꝉ

Published: Nov. 26, 2021

Multicomponent reactions (MCRs) provide an alternative scheme for target synthesis, by allowing fast and efficient synthetic access based on its "one-pot" character, accessing almost unlimited scaffold diversity, fostering a very large chemical space simple building blocks available in numerous derivatives, addressing challenging issues of sustainability ("green chemistry"). Hence, MCR can be potentially useful the discovery synthesis biologically active "drug-like" compounds. Here, we highlight examples use medicinal chemistry, from drug discovery, drugs, to screening libraries biopharmaceutical applications. The review is not comprehensive but rather personal selection authors reader overview advantages usefulness MCR. We conclude that literature analysis, toto , supports highly underused role chemistry.

Language: Английский

A Mini Review on the Multicomponent Synthesis of Pyridine Derivatives DOI

Lokesh Kumar S,

Sumaiya Tabassum,

Kunigal S. Sagar

et al.

ChemistrySelect, Journal Year: 2022, Volume and Issue: 7(47)

Published: Dec. 14, 2022

Abstract Multicomponent reactions (MCRs) have emerged as key green tool in organic synthesis for their methodological simplicity. MCRs made heterocycle more versatile. The most crucial molecule among the often used heterocycles is pyridine, which widely biological, industrial, and pharmaceutical sectors. In light of this, our mini‐review highlights literature on substituted pyridine published from year 2016 to early 2022 via multicomponent approach.

Language: Английский

Citations

20

Recent progress in the Cu-catalyzed multicomponent synthesis of 1,4-disubstituted 1,2,3-triazoles DOI

Akash Anand,

Rajneesh Kumar,

Jyotirmoy Maity

et al.

Synthetic Communications, Journal Year: 2023, Volume and Issue: 53(5), P. 345 - 375

Published: Feb. 3, 2023

1,2,3-Triazoles has emerged as one of the most important N-heterocyclic compounds with a broad range pharmacological applications. This class molecules can accommodate wide substituents or groups around core moiety that pave mode for synthesis various bioactive compounds. Copper(I)-catalyzed azide-alkyne cycloaddition reaction become leading click chemistry methodologies due to its high biocompatibility, reliability, and specificity. 1,4-Disubstituted 1,2,3-triazoles via multicomponent generated numerous biological interest in an efficient manner. review summarizes recent literature on regioselective 1,4-disubstituted copper-catalyzed reactions since 2018.

Language: Английский

Citations

12

Oxygen-, Nitrogen-, and Sulfur-Containing Heterocycles: Recent Advances in De Novo Synthesis and Prospect DOI
Yongpeng Zheng, Jianxiao Li, Wanqing Wu

et al.

Organic Process Research & Development, Journal Year: 2024, Volume and Issue: 28(8), P. 2988 - 3025

Published: July 13, 2024

Language: Английский

Citations

4

An attractive approach to access 1,2,4-oxadiazole derivatives based on developing a novel carbon nanotube-magnetic catalyst DOI

Zemiao Yin,

Zenghao Zhang,

Yiting Fu

et al.

Journal of Molecular Structure, Journal Year: 2025, Volume and Issue: unknown, P. 142050 - 142050

Published: March 1, 2025

Language: Английский

Citations

0

Dioxazolones as electrophilic amide sources in copper-catalyzed and -mediated transformations DOI Creative Commons

Seungmin Lee,

Minsuk Kim,

Hyewon Han

et al.

Beilstein Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: 21, P. 200 - 216

Published: Jan. 22, 2025

Over the past decade, dioxazolones have been widely used as N -acylamide sources in amidation processes of challenging substrates, typically employing precious transition metals. However, these catalytic systems often present several challenges associated with cost, toxicity, stability, and recyclability. Among 3d metals, copper catalysts gaining increasing attention owing to their abundance, cost-effectiveness, sustainability. Recently, applied chemical transformation dioxazolones, conferring a convenient protocol towards amidated products. This review highlights recent advancements synthetic transformations particular examples salts.

Language: Английский

Citations

0

CuI-Catalyzed Dearomatization/Peroxidation/Cyclization Cascade of Pyrrole-Tethered Indoles DOI

Xue Sheng,

Yang Liu,

Jiayi Han

et al.

The Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 27, 2025

A mild CuI-catalyzed dearomatization/peroxidation/cyclization cascade of pyrrole-tethered indoles has been reached, providing peroxide-incorporated indolizino[8,7-b]indole derivatives in acceptable to good yields (46–76%). Dehydrogenated peroxide can be obtained by the use a FeCl3/TBHP (tBuOOH)/2,2,2-trifluoroethanol (TFE) system at 50 °C.

Language: Английский

Citations

0

Sustainable copper nanocomposite for multicomponent synthesis of triazolo quinolines and triazolyl benzamide derivatives and their bioactivity study DOI

R. Nandini,

Byresh B. Kempegowda,

Sudhanva M. Srinivasa

et al.

Catalysis Science & Technology, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

Herein, we report an efficient methodology for the preparation of a heterogeneous sustainable magnetically separable Cu@PANI@Fe 3 O 4 nanocomposite, and its catalytic efficiency in multicomponent reactions synthesis triazolo quinolines triazolyl benzamide derivatives is investigated.

Language: Английский

Citations

0

Grindstone chemistry: A “green” approach for the synthesis and derivatization of heterocycles DOI
Mainak Banerjee,

Padmini C. Panjikar,

Dharmendra Das

et al.

Tetrahedron, Journal Year: 2022, Volume and Issue: 112, P. 132753 - 132753

Published: April 1, 2022

Language: Английский

Citations

15

Synthesis Strategies and Medicinal Value of Pyrrole and its Fused Heterocyclic Compounds DOI

Samar S. Fatahala,

Mosaad S. Mohamed,

Jaqueline Youssef Sabry

et al.

Medicinal Chemistry, Journal Year: 2022, Volume and Issue: 18(10), P. 1013 - 1043

Published: March 26, 2022

In the last several decades, interest in pyrrole and pyrrolopyrimidine derivatives has increased owing to their biological importance, such as anti-tumor, anti-microbial, anti-inflammatory, anti-diabetic, anti-histaminic, anti-malarial, anti-Parkinson, antioxidant anti-viral effects, specially recently against COVID-19. These tremendous features have motivated scientists discover more fused derivatives, great importance of nucleus a pharmacophore many drugs, us present this article, highlighting on different synthetic pathways its compounds, pyrrolopyrimidine, well medicinal value from 2017 till 2021.

Language: Английский

Citations

13

Brønsted-acidic ionic liquid supported nanomagnetic: a novel and reusable catalyst for synthesis of oxygen-containing heterocyclic compounds DOI
Masoomeh Norouzi,

Maryam Khanmoradi

Research on Chemical Intermediates, Journal Year: 2023, Volume and Issue: 49(11), P. 4785 - 4804

Published: Aug. 19, 2023

Language: Английский

Citations

8