MICROWAVE-ASSISTED FUNCTIONALIZATION OF INDAZOLES: AN OVERVIEW DOI Open Access
Subrata Mondal

RASAYAN Journal of Chemistry, Journal Year: 2023, Volume and Issue: 16(03), P. 1560 - 1574

Published: Jan. 1, 2023

Indazole-based heterocyclic compounds possessing significant medicinal properties form the basis of developing several pharmaceuticals.Microwave-assisted organic synthesis is one most effective and promising techniques from perspective green chemistry, as it increases reaction rates yields while decreasing wasteful byproducts.Functionalization indazole derivatives under microwave irradiation achieving tremendous interest in recent times.Various cross-coupling reactions are generally utilized during microwave-assisted functionalization indazoles.This review article chronologically describes different types indazoles assisted by with up-to-date literature coverage.

Language: Английский

Design, synthesis and antimicrobial activity of novel quinoline-2-one hybrids as promising DNA gyrase and topoisomerase IV inhibitors DOI
Mohammed A. I. Elbastawesy, Fatma A. Mohamed, Islam Zaki

et al.

Journal of Molecular Structure, Journal Year: 2023, Volume and Issue: 1278, P. 134902 - 134902

Published: Jan. 3, 2023

Language: Английский

Citations

11

Recent Strategies in Nickel-Catalyzed C–H Bond Functionalization for Nitrogen-Containing Heterocycles DOI Open Access
Ke Yang, Zhi Li,

Qingyue Hu

et al.

Catalysts, Journal Year: 2022, Volume and Issue: 12(10), P. 1163 - 1163

Published: Oct. 2, 2022

N-heterocycles are ubiquitous in natural products, pharmaceuticals, organic materials, and numerous functional molecules. Among the current synthetic approaches, transition metal-catalyzed C–H functionalization has gained considerable attention recent years due to its advantages of simplicity, high atomic economy, ready availability starting materials. In field N-heterocycle synthesis via functionalization, nickel been recognized as one most important catalysts. this review, we will introduce nickel-catalyzed intramolecular intermolecular pathways for from 2008 2021.

Language: Английский

Citations

12

Recent advances in phosphine-mediated sequential annulations DOI

Xuling Pan,

Wei Cai, You Huang

et al.

Chinese Chemical Letters, Journal Year: 2024, Volume and Issue: unknown, P. 110628 - 110628

Published: Nov. 1, 2024

Language: Английский

Citations

1

Photo- and Electro-chemical Strategies for Indazole Synthesis DOI Creative Commons
Binbin Huang

Tetrahedron Chem, Journal Year: 2024, Volume and Issue: unknown, P. 100116 - 100116

Published: Dec. 1, 2024

The indazole core is prevalently found in the structures of bioactive molecules, demonstrating promising potential medicinal chemistry and drug discovery, which therefore has attracted sustained attention from synthetic community. Over recent decades, significant progress been achieved both organic photocatalysis electrosynthesis, offering novel approaches for efficient sustainable synthesis various functionalized indazoles. This mini-review highlights emerging methodological advancements photo-/electro-chemical two common forms indazole, namely 1H- 2H-indazoles, are classified by specific intramolecular bond formation patterns: (1) C-C formation, (2) C-N (3) N-N formation. reaction conditions, representative scopes, mechanistic understandings these protocols emphasized, to elucidate advantages limitations current strategies, with an aim inspire future innovations that may address challenges modern synthesis.Graphical abstractTo create your abstract, type over instructions template box below. Fonts or abstract dimensions should not be changed altered.

Language: Английский

Citations

1

Recent Advances in the Light-assisted Synthesis of Ring Junction Nitrogen Heterocycles DOI

Periasamy Vinoth Kumar,

Kumar Aravindraj,

Gunabalan Madhumitha

et al.

Current Organic Chemistry, Journal Year: 2023, Volume and Issue: 27(12), P. 997 - 1009

Published: June 1, 2023

Abstract: Nitrogen ring junction heterocycles play a crucial role in synthetic organic chemistry due to their remarkable activity. The fused nitrogen compounds are abundant nature; they have excellent biological activity and used against various health issues. To make selective products from the heterocycles, expensive chemicals catalysts, like transition metal complexes composites, required. neglect drawbacks of conventional synthesis methods long reaction times, by-product formation, lower selectivity, low yields, an alternative nonconventional light-mediated techniques can be opted for. light source uses radical mechanism that reduces provides regio-selective product, increases yield, decreases time, is cost-effective, does not require special catalysts or chemicals. There variety sources, viz., UV, visible, IR, laser, X-ray. visible light, white, green, blue LED sources widely photochemical method. This review emphasizes nitrogen-ring heterocyclic compounds.

Language: Английский

Citations

3

Access to Fully Substituted Dihydroindazoles Via Hexadehydro-Diels–Alder/[3 + 2] Cycloaddition DOI
Weigang Xu,

Xiuhuan Li,

Luyao Zou

et al.

The Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 88(20), P. 14736 - 14747

Published: Oct. 11, 2023

A cascade hexadehydro-Diels–Alder (HDDA)/[3 + 2] cycloaddition reaction between tetrayne and N,N′-cyclic acylhydrazone is described. This strategy allows the efficient construction of fully substituted 2,3-dihydro-1H-indazole scaffolds which have insecticidal activity against third instar larvae Mythimna separata.

Language: Английский

Citations

3

Synthesis of Substituted Indazole Acetic Acids by N−N Bond Forming Reactions DOI Creative Commons
Luke R. Odell, Bobo Skillinghaug,

Christof Matt

et al.

European Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 26(29)

Published: May 11, 2023

Abstract Herein, we report on the discovery and development of novel cascade N−N bond forming reactions for synthesis rare indazole acetic acid scaffolds. This approach allows convenient three distinct derivatives (unsubstituted, hydroxy, alkoxy) by heating 3‐amino‐3‐(2‐nitroaryl)propanoic acids with an appropriate nucleophile/solvent under basic conditions. The reaction tolerates a range functional groups electronic effects and, in total, 23 were synthesized characterized. work offers valuable strategy useful scaffolds drug programs.

Language: Английский

Citations

2

Construction of Nitrogen-Containing Heterocycles via Nickel-Catalyzed C–H Bond Functionalization Processes DOI

Robbie Ge,

Ke Yang, Haibo Ge

et al.

Topics in heterocyclic chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 211 - 233

Published: Jan. 1, 2024

Language: Английский

Citations

0

Additive-Controlled Divergent Synthesis of Fluorenone-4-carboxylic Acids and Diphenic Anhydrides via Rhodium-Catalyzed Oxidative Dimeric Cyclization of Aromatic Acids DOI

Wan-Di Li,

Xue Wang,

Hong-Yu Ma

et al.

Organic Letters, Journal Year: 2024, Volume and Issue: 26(36), P. 7607 - 7613

Published: Sept. 4, 2024

A rhodium-catalyzed one-pot access to valuable polycyclic frameworks of fluorenone-4-carboxylic acids and diphenic anhydrides via the oxidative dimeric cyclization aromatic has been developed. This transformation proceeded carboxyl-assisted 2-fold C-H activation followed by intramolecular Friedel-Crafts or dehydration reactions. The silver salt additive plays a vital role in chemoselectivity products. Diphenic anhydride

Language: Английский

Citations

0

Eco-friendly, green and new metal-free intramolecular Friedel–Crafts reaction to synthesis of Acridones derivatives using phenylboronic acid derivatives DOI

Mohammad Askarzadeh,

Ali Moazzam, Mohammad Hosein Sayahi

et al.

Tetrahedron Letters, Journal Year: 2023, Volume and Issue: 123, P. 154532 - 154532

Published: May 4, 2023

Language: Английский

Citations

1