Rhodium-Catalyzed Direct Vinylene Annulation of 2-Aryloxazolines and Cascade Ring-Opening Using a Vinyl Selenone DOI
Yuji Nishii, Masahiro Miura,

Junya Kitano

et al.

Synlett, Journal Year: 2023, Volume and Issue: unknown

Published: Nov. 20, 2023

Abstract Over the past two decades, transition-metal-catalyzed C–H activation and subsequent oxidative cyclization with alkynes or their surrogates has emerged as a powerful synthetic tool for fused heteroaromatics. We report Rh(III)-catalyzed annulation ring-opening cascade reaction 2-aryloxazolines. By utilizing vinyl selenone an oxidizing acetylene surrogate, target three-component coupling products were obtained in high yields without using stoichiometric amount of external oxidant.

Language: Английский

Accelerated photochemical reactions at oil-water interface exploiting melting point depression DOI
Ya‐Ming Tian, Wagner Silva, Ruth M. Gschwind

et al.

Science, Journal Year: 2024, Volume and Issue: 383(6684), P. 750 - 756

Published: Feb. 15, 2024

Water can accelerate a variety of organic reactions far beyond the rates observed in classical solvents. However, using pure water as solvent introduces solubility constraints that have limited applicability efficient photochemistry particular. We report here formation aggregates between pairs arenes, heteroarenes, enamines, or esters with different electron affinities an aqueous medium, leading to oil-water phase boundary through substrate melting point depression. The active hydrogen atoms reactants engage bonds water, thereby accelerating photochemical reactions. This methodology realizes appealingly simple conditions for coupling complex solid molecules, including drug molecules are poorly soluble water.

Language: Английский

Citations

33

Ruthenium-catalyzed oxidative coupling of vinylene carbonate with isoxazoles: access to fused anthranils DOI
Pravin Kumar, Manmohan Kapur

Chemical Communications, Journal Year: 2022, Volume and Issue: 58(28), P. 4476 - 4479

Published: Jan. 1, 2022

A ruthenium-catalyzed oxidative coupling of vinylene carbonate with isoxazoles has been developed to achieve the direct C-H formylmethylation a diverse array arylisoxazoles utilizing isoxazole ring as directing group. simple manipulation established reaction conditions leads formation fused-anthranils. Importantly, functions both formylmethyl cation equivalent through decarboxylation process and an acetylene equivalent. Control experiments were conducted elucidate plausible mechanism. This methodology is expected provide facile expeditious approach for synthesis

Language: Английский

Citations

25

Advancement of vinylene carbonate as a coupling partner in metal-catalyzed C–H functionalization DOI

Yicong Ge,

Qiang Yan,

Jiang Nan

et al.

Organic Chemistry Frontiers, Journal Year: 2023, Volume and Issue: 10(22), P. 5717 - 5734

Published: Jan. 1, 2023

Vinylene carbonate (VC) has emerged as a promising coupling partner to participate in various attractive C–H conversions and implement an increasing number of novel reactions. In this review, we provide summary the advancements achieved metal-catalyzed functionalization using VC.

Language: Английский

Citations

16

Rhodium‐Catalyzed Direct Vinylene Annulation of Sulfoxonium Ylides and N‐carbamoylindoles with Vinylene Carbonate DOI

Jia‐Lin Song,

Lin Xiao,

Shaoyong Chen

et al.

Advanced Synthesis & Catalysis, Journal Year: 2023, Volume and Issue: 365(9), P. 1457 - 1464

Published: April 14, 2023

Abstract In this study, Rh(III)‐catalyzed C−H bifunctionalization and direct vinylene annulation of sulfoxonium ylides N ‐carbamoylindoles with carbonate was accomplished, which afforded a series naphthalenones containing β‐ketosulfoxonium ylide moiety, isocoumarins, pyrimidones. This protocol featured mild conditions, broad substrate scope, functional‐groups compatibility. addition, related applications preliminary mechanistic exploratory were also investigated magnified image

Language: Английский

Citations

14

Rhodium-Catalyzed Isoquinoline Synthesis Using Vinyl Selenone as Oxidizing Acetylene Surrogate DOI

Ayumi Inami,

Yuji Nishii, Koji Hirano

et al.

Organic Letters, Journal Year: 2023, Volume and Issue: 25(18), P. 3206 - 3209

Published: May 4, 2023

Isoquinoline is a privileged structure in many bioactive compounds and valuable ligands. Transition-metal-catalyzed oxidative annulation of imine derivatives has become promising synthetic method; however, catalytic synthesis 3,4-nonsubstituted isoquinolines by formal acetylene been scarce to date. Herein, we introduce vinyl selenone as an effective surrogate for the Rh-catalyzed annulative coupling under mild conditions. The Se fragment can be recovered diselenide recycled. product readily converted 1-aminoisoquinolines.

Language: Английский

Citations

11

Vinylene Carbonate as Synthon in Transition Metal‐Catalyzed C−H Bond Activation/Annulation Reactions DOI Open Access

Xiaofan Cui,

Rémi Chauvin, Chao Pi

et al.

Advanced Synthesis & Catalysis, Journal Year: 2023, Volume and Issue: 365(20), P. 3400 - 3412

Published: Sept. 6, 2023

Abstract Recently, vinylene carbonate has been developed as a powerful synthon in transition metal‐catalyzed C−H bond activation/cyclization reactions. This review introduces recent progress the use of reactant, by analyzing and comparing reaction models involving surrogate ethynol, acetylene, acetylation reagents or other reactants, while addressing related mechanisms synthetic applications.

Language: Английский

Citations

11

Copper-catalyzed aerobic photodecarboxylation of carboxylic acids to aldehydes and ketones DOI Creative Commons

Yonghuan Wang,

Biping Xu,

Xuan Xiao

et al.

Green Synthesis and Catalysis, Journal Year: 2025, Volume and Issue: unknown

Published: March 1, 2025

Language: Английский

Citations

0

Green Synthesis of 3,4‐Unsubstituted Isoquinolones through Rhodium(III)‐Catalyzed C−H Activation and Annulation in Ethanol DOI
Vikash Kumar, Parthasarathy Gandeepan

European Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 26(44)

Published: Sept. 27, 2023

Abstract A mild and convenient synthesis of 3,4‐unsubstituted isoquinolones has been achieved from N ‐methoxybenzamides vinylene carbonate as an acetylene surrogate with a versatile rhodium(III) catalyst. The reaction proceeded at room temperature in biomass derived ethanol solvent. This protocol avoids the use stoichiometric external oxidant, served internal oxidant. C−H/N−H activation annulation manifold broad substrate scope excellent levels regioselectivities. preliminary mechanistic studies suggest facile reversible chelation‐assisted C−H rhodation. Diversification provide access to 4‐substituted isoquinolines, which are complementary previously reported protocols.

Language: Английский

Citations

8

Diversely functionalized isoquinolines and their core-embedded heterocyclic frameworks: a privileged scaffold for medicinal chemistry DOI

Archana Vijayakumar,

M. Manod,

Raveendran Bharath Krishna

et al.

RSC Medicinal Chemistry, Journal Year: 2023, Volume and Issue: 14(12), P. 2509 - 2534

Published: Jan. 1, 2023

This review will be an essential toolbox for medicinal and bioorganic chemists seeking novel multifunctional hybrid bioactive N-heterocycles drug discovery. The work highlights the need relevance of unexplored bioisosterism employing isoquinoline-based small-molecules in design.

Language: Английский

Citations

7

Recent Advances in the 3 d‐Transition‐Metal‐Catalyzed Synthesis of Isoquinolines and its Derivatives DOI
Vipin K. Maikhuri, Manish Rawat, Diwan S. Rawat

et al.

Advanced Synthesis & Catalysis, Journal Year: 2023, Volume and Issue: 365(24), P. 4458 - 4494

Published: Nov. 24, 2023

Abstract The preservation of scarce rare earth metals, such as palladium, rhodium, iridium, and others, poses a significant challenge for humanity due to their limited availability. These metals might be replaced by earth‐abundant 3d‐transition cobalt, manganese, iron, nickel, copper, etc . Isoquinolines have acquired an important position in synthetic organic chemistry well medicinal chemistry. They manifest diverse range natural molecules, serving pivotal synthons the synthesis numerous bioactive compounds with notable significance. Numerous reports on isoquinoline derivatives via transition metal catalysis been published worldwide. In this review, we summarize recent approaches synthesizing various using 3d‐transition‐metal catalysts since 2020. review has divided into different 3d‐transition‐metal‐based catalysis. We expect that will bring better overview present status progress made isoquinolines persuade more advancements research area near future.

Language: Английский

Citations

7