A Detailed Review on the Synthesis and Mechanistic Study of Pyrrole Fused Quinone/Naphthoquinone DOI
Susanta Kumar Manna,

Sampa Mondal,

Tapas Ghosh

et al.

ChemistrySelect, Journal Year: 2024, Volume and Issue: 9(46)

Published: Dec. 1, 2024

Abstract This review article intends to explore the versatility in formation of pyrrole‐fused quinone/naphthoquinone derivatives described literature from 2008 2024. It deals with multitude paths its synthesis a variety precursors using both metal‐ and metal‐free catalytic systems their potential applications. also documented several bioactive cores accommodating indoloquinone analog. Noteworthy, mitomycin A acts as excellent medicine for cancer treatment analog EO‐9 is under clinical trial. Here we present natural products zyzzyanone A, murrayaquinones B indolequinone‐based naloxone prodrugs exiguamine (NQO1)‐targeted hypoxia specific activation, antibiotic uthamycin analog, indolequinone fused ursolic acid (a triterpenoid rich many Chinese medicines), which vital scaffold preparation novel anticancer agent. Indoloquinone‐fused medicines) Recent two cyanobacterial metabolites Calothrixins has been documented. discusses intermediate, where lymphostin alkaloid can be developed. Lamellarin D product easily prepared by developed strategy.

Language: Английский

Synthesis, characterization and sensor applications of a new 1,4-naphthoquinone derivative molecule DOI
Oğuz Özbek, Onur Cem Altunoluk, Kıymet Berkil Akar

et al.

Chemical Papers, Journal Year: 2025, Volume and Issue: unknown

Published: March 18, 2025

Language: Английский

Citations

1

Co(III)-Catalyzed Regioselective Functionalization of Isoquinolones with Naphthoquinones DOI
Tamanna Sharma,

Sumit Sharma,

Sachin

et al.

Organic Letters, Journal Year: 2024, Volume and Issue: 26(23), P. 5027 - 5031

Published: June 3, 2024

A strategy for Co(III)-catalyzed C(sp

Language: Английский

Citations

4

Current status of 1,4-Naphthoquinones and their derivatives for wound healing DOI Creative Commons
Pooja Kumari, Vikramjeet Singh, Vinay Kant

et al.

European Journal of Medicinal Chemistry Reports, Journal Year: 2024, Volume and Issue: 12, P. 100194 - 100194

Published: July 27, 2024

Cutaneous wounds are a major healthcare concern affecting millions of people as they fail to heal properly and can result in life threatening conditions high economic loss. Wound healing is complex, multifaceted process involving four consequent stages: haemostasis, inflammation, proliferation, tissue remodelling. These phases work coordination restore the integrity damaged skin underlying tissues. 1,4-Naphthoquinone compounds their derivatives have emerged promising candidates wound management. Herein, natural such lawsone, juglone, shikonin, plumbagin along with been discussed for potential special emphasis on structural activity relationships. This review provides comprehensive discussion chemical reactivity, biological activities, mechanisms action these naphthoquinone-based compounds, particularly antibacterial properties, which play crucial role healing. The highlights importance elucidating structure-activity relationships overcome challenges associated poor solubility, low efficacy, presence inevitable impurities plant extracts. Additionally, emphasizes significance developing diverse naphthoquinone at laboratory scale expand repertoire agents.

Language: Английский

Citations

4

Catalyst-free, one-pot four-component synthesis of aryl-linked hydroxy-naphthoquinone fused with imidazolone and 2-hydroxy-1,4-naphthoquinone moiety: naphtho[1,2-d]imidazolyl(aryl)methylnaphthalene-1,4-diones DOI Creative Commons

Mohaddeseh Ahmadusefi-Sarhadi,

Hossein Mehrabi,

Farzaneh Alizadeh‐Bami

et al.

Results in Chemistry, Journal Year: 2025, Volume and Issue: unknown, P. 102057 - 102057

Published: Jan. 1, 2025

Language: Английский

Citations

0

Antimycobacterial compounds isolated from medicinal plants: A South African comprehensive review DOI Creative Commons
N.I. Mongalo, Maropeng Vellry Raletsena

South African Journal of Botany, Journal Year: 2025, Volume and Issue: 181, P. 236 - 257

Published: April 22, 2025

Language: Английский

Citations

0

Design, synthesis, and in vitro and in vivo biological evaluation of 2-amino-naphtho[2,3-b]thiophene-4,9-dione derivatives as potent anticancer agents. DOI

Soumen k. Manik,

Satyajit Haldar,

Ankita Bhattachrya

et al.

European Journal of Medicinal Chemistry, Journal Year: 2025, Volume and Issue: unknown, P. 117728 - 117728

Published: May 1, 2025

Language: Английский

Citations

0

2-Amino-1,4-naphthoquinone as a key precursor for naphthoquinone-fused N-heterocycles: synthetic approaches and mechanistic perspectives DOI

Ujjain Chaurasia,

Tasneem Parvin

Molecular Diversity, Journal Year: 2025, Volume and Issue: unknown

Published: May 14, 2025

Language: Английский

Citations

0

1,4-Naphthoquinone thiazoles: Synthesis, crystal structure, anti-proliferative activity, and inverse molecular docking study DOI
Çağla Efeoğlu, Rıza Serttas, Bünyamin Demır

et al.

Journal of Molecular Structure, Journal Year: 2024, Volume and Issue: 1322, P. 140330 - 140330

Published: Oct. 9, 2024

Language: Английский

Citations

2

Synthesis of Aryl Naphthoquinones and Maleimides via Pd(II)‐Catalyzed Template‐Assisted m‐C(sp2)‐H Functionalization Reaction DOI
Masilamani Jeganmohan, Ananya Dutta

Chemistry - A European Journal, Journal Year: 2024, Volume and Issue: 30(59)

Published: Aug. 12, 2024

An efficient approach for the synthesis of substituted aryl naphthoquinones via a Pd(II)-catalyzed template-assisted m-C(sp

Language: Английский

Citations

0

Synthesis of 1,4‐Naphthoquinones via Palladium(II)‐Catalyzed Tertiary C−H Alkylation of Olefins Followed by C−C Bond Cleavage DOI
Xu Zhang,

Mengfan Chang,

Tongtong Ni

et al.

European Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 28, 2024

Abstract An efficient method has been developed for the preparation of 1,4‐naphthoquinones via a palladium‐catalyzed reaction 2‐aryl‐1,3‐indandiones with olefins. This involves tertiary C−H alkylation olefins to produce alcohol, followed by C−C bond cleavage.

Language: Английский

Citations

0