Synthesis of 3-Aroyl-4-heteroarylpyrrole Derivatives by the Van Leusen Method DOI Creative Commons
Jorge Trilleras, Jairo Quiroga, Angelina Hormaza

и другие.

Molbank, Год журнала: 2022, Номер 2022(1), С. M1341 - M1341

Опубликована: Фев. 15, 2022

The synthesis and structural diversification of N-heterocycles systems have attracted much attention because their potential applications. Three 6-aryl-3-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde 4 derivatives, in reaction with acetophenones 5, via conventional Claisen–Schmidt condensation reactions, generated the respective enones. enones were used as electron-deficient olefins a “formal” [2+3] cycloaddition using p-tosylmethyl isocyanide—TosMIC 7. This protocol allows access to 3-(substituted aroyl)-4-heteroaryl pyrrole derivatives by Van Leusen method.

Язык: Английский

Multicomponent Reaction-Assisted Drug Discovery: A Time- and Cost-Effective Green Approach Speeding Up Identification and Optimization of Anticancer Drugs DOI Open Access
Giovanni Graziano, Angela Stefanachi, Marialessandra Contino

и другие.

International Journal of Molecular Sciences, Год журнала: 2023, Номер 24(7), С. 6581 - 6581

Опубликована: Апрель 1, 2023

Multicomponent reactions (MCRs) have emerged as a powerful strategy in synthetic organic chemistry due to their widespread applications drug discovery and development. MCRs are flexible transformations which three or more substrates react form structurally complex products with high atomic efficiency. They being increasingly appreciated highly exploratory evolutionary tool by the medicinal community, opening door sustainable, cost-effective rapid synthesis of biologically active molecules. In recent years, MCR-based strategies found extensive application field discovery, several anticancer drugs been synthesized through MCRs. this review, we present an overview representative literature examples documenting different approaches development new drugs.

Язык: Английский

Процитировано

46

Pyrrole: A Decisive Scaffold for the Development of Therapeutic Agents and Structure‐Activity Relationship DOI

Bharathi Hassan Ganesh,

Anirudh G. Raj, Baladhandapani Aruchamy

и другие.

ChemMedChem, Год журнала: 2023, Номер 19(1)

Опубликована: Ноя. 6, 2023

An overview of pyrroles as distinct scaffolds with therapeutic potential and the significance pyrrole derivatives for drug development are provided in this article. It lists instances naturally occurring pyrrole-containing compounds describes sources nature, including plants microbes. also explains many conventional modern synthetic methods used to produce pyrroles. The key topics biological characteristics, pharmacological behavior, functional alterations displayed by derivatives. details how treat infectious diseases. disorders resistant standard treatments discusses function containing combating Furthermore, review covers uses treating non-infectious diseases resistance mechanisms illnesses like cancer, diabetes, Alzheimer's Parkinson's important discoveries probable avenues research finally summarized, along their medicinal chemists development. A reference from last two decades is included review.

Язык: Английский

Процитировано

33

Green and efficient one-pot three-component synthesis of novel drug-like furo[2,3-d]pyrimidines as potential active site inhibitors and putative allosteric hotspots modulators of both SARS-CoV-2 MPro and PLPro DOI Open Access
Hossein Mousavi, Behzad Zeynizadeh, Mehdi Rimaz

и другие.

Bioorganic Chemistry, Год журнала: 2023, Номер 135, С. 106390 - 106390

Опубликована: Янв. 28, 2023

Язык: Английский

Процитировано

28

Cyanation with isocyanides: recent advances and perspectives DOI

Yingying Shan,

Xun Zhang,

Gongle Liu

и другие.

Chemical Communications, Год журнала: 2024, Номер 60(12), С. 1546 - 1562

Опубликована: Янв. 1, 2024

This review focuses on the cyanation of isocyanides with recent advances and perspectives.

Язык: Английский

Процитировано

11

Isocyanide-Based Multicomponent Reactions in Water: Advanced Green Tools for the Synthesis of Heterocyclic Compounds DOI

Tahereh Nasiriani,

Siamak Javanbakht, Mohammad Taghi Nazeri

и другие.

Topics in Current Chemistry, Год журнала: 2022, Номер 380(6)

Опубликована: Сен. 22, 2022

Язык: Английский

Процитировано

32

Click reaction inspired synthesis, antimicrobial evaluation and in silico docking of some pyrrole-chalcone linked 1,2,3-triazole hybrids DOI

Monika Yadav,

Kashmiri Lal, Aman Kumar

и другие.

Journal of Molecular Structure, Год журнала: 2022, Номер 1273, С. 134321 - 134321

Опубликована: Окт. 12, 2022

Язык: Английский

Процитировано

30

Sustainable Synthesis of Pseudopeptides via Isocyanide-Based Multicomponent Reactions in Water DOI
Mohammad Taghi Nazeri,

Tahereh Nasiriani,

Hassan Farhid

и другие.

ACS Sustainable Chemistry & Engineering, Год журнала: 2022, Номер 10(25), С. 8115 - 8134

Опубликована: Май 26, 2022

The impressive success in the synthesis of novel products via sustainable and green methods is a crucial purpose organic synthesis. Water as "green solvent" plays vital role accelerating some reactions, displaying unique reactivity selectivity from conventional solvents. isocyanide-based multicomponent reactions (I-MCRs) versatile have received significant consideration pseudopeptidic frames, especially drug discovery. This because nature isocyanides that play special active reactant. I-MCRs water solvent reagent for compounds become an interesting research direction, enabling simultaneous growth both solvents toward ideal reaction rate was accelerated due to lower activation volumes condensation several reactants into single reactive intermediate product. Furthermore, executed possibly are mild, easily controlled, environmentally friendly, which conform well "Green Chemistry" principles. On other hand, these powerful syntheses aqueous media perpetuated by acceleration reduction number workups, purification, extraction steps. main subject this review performed pseudopeptide structures. It deserves be pointed out whereas progress has been recently made on MCRs transformations, there no exclusive account focus publish about eco-friendly pseudopeptides. Nevertheless, we hope themed assemblage will attractive useful pharmaceutical chemists encourage more development fascinating engaging field.

Язык: Английский

Процитировано

28

Modular Synthesis of Tetrasubstituted Pyrroles through a Four-Component Cyclization Strategy Using Ammonium Salt as the Nitrogen Source DOI

Chunlan Zhou,

Haolin Zheng,

Ya Chen

и другие.

The Journal of Organic Chemistry, Год журнала: 2023, Номер 88(3), С. 1533 - 1544

Опубликована: Янв. 19, 2023

A four-component synthesis of tetrasubstituted pyrroles was developed under metal-free conditions. The pyrrole ring formed in one pot through [2 + 1 1] condensation using ammonium salt as the nitrogen source. In this strategy, 1,4-naphthoquinones and maleimides were used versatile C2 fragments to provide substituted benzo[f]isoindole-4,9-diones pyrrolo[3,4-c]pyrrole-1,3-diones, respectively. This work is highlighted by source, readily available starting materials multibond formation (two C–C two C–N bonds) a single operation.

Язык: Английский

Процитировано

12

Catalytic metal-enabled story of isocyanides for use as “C1N1” synthons in cyclization: beyond radical chemistry DOI
Dianpeng Chen, Jianming Li, Xin Wang

и другие.

Organic Chemistry Frontiers, Год журнала: 2022, Номер 9(15), С. 4209 - 4220

Опубликована: Янв. 1, 2022

This review summarizes recent advances in the use of isocyanide as “C1N1” synthons cyclization.

Язык: Английский

Процитировано

18

Transition‐Metal‐Free Synthesis of N‐Heterocyclic Compounds via Multi‐Component Reactions DOI Open Access

Dhruba Jyoti Boruah,

Lodsna Borkotoky,

Uma Devi Newar

и другие.

Asian Journal of Organic Chemistry, Год журнала: 2023, Номер 12(9)

Опубликована: Июль 29, 2023

Abstract Multicomponent reactions (MCRs) have emerged as powerful tools in synthetic chemistry for the efficient synthesis of diverse molecular scaffolds, particularly nitrogen‐containing heterocycles. Despite their numerous advantages, use transition metal catalysts or additives MCRs can present limitations due to cost, toxicity, and environmental concerns. In recent years, there has been a growing interest metal‐free N ‐heterocyclic compounds. This review provides comprehensive concise overview advancements valuable ‐heterocycles over past five years. The is systematically organized, categorizing discussed based on size heterocyclic ring number nitrogen atoms. Only that result formation rings containing at least one atom are included, while derivatization using falls outside scope this review. By highlighting developments field, aims showcase potential significance sustainable strategies accessing elimination metals not only simplifies reaction conditions but also contributes greener more environmentally friendly approaches. serves resource researchers interested design application

Язык: Английский

Процитировано

11