4.8 Article

Ni-Catalyzed Aryl Sulfide Synthesis through an Aryl Exchange Reaction

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Review Chemistry, Multidisciplinary

Selective Decarbonylation via Transition-Metal-Catalyzed Carbon- Carbon Bond Cleavage

Hong Lu et al.

Summary: Transition-metal-catalyzed decarbonylation via carbon-carbon bond cleavage is a crucial synthetic methodology. This method offers a distinct synthetic strategy using carbonyl groups as traceless handles. Significant progress has been made in recent years in various aspects of this reaction.

CHEMICAL REVIEWS (2021)

Article Chemistry, Organic

Decarbonylative Synthesis of Aryl Nitriles from Aromatic Esters and Organocyanides by a Nickel Catalyst

Keiichiro Iizumi et al.

Summary: A decarbonylative cyanation of aromatic esters with aminoacetonitriles in the presence of a nickel catalyst was developed using a thiophene-based diphosphine ligand, dcypt, to synthesize aryl nitrile without generating stoichiometric metal- or halogen-containing chemical wastes. A wide range of aromatic esters, including hetarenes and pharmaceutical molecules, can be converted into aryl nitriles.

SYNLETT (2021)

Article Chemistry, Multidisciplinary

Nickel-Catalyzed Reversible Functional Group Metathesis between Aryl Nitriles and Aryl Thioethers

Tristan Delcaillau et al.

Summary: A new functional group metathesis reaction between aryl nitrites and aryl thioethers has been described, utilizing a catalytic system of nickel/dcype to achieve fully reversible transformation in good to excellent yields. This cyanide- and thiol-free reaction demonstrates high functional group tolerance and efficiency for late-stage derivatization of commercial molecules, with synthetic applications showcasing its versatility and utility in multistep synthesis.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2021)

Review Chemistry, Multidisciplinary

Visible light photocatalysis in the late-stage functionalization of pharmaceutically relevant compounds

Rolando Cannalire et al.

Summary: Late stage functionalization is a powerful tool for accelerating the identification of structure-activity relationships and optimizing ADME profiles of drugs. Visible-light photocatalysis offers a smooth and clean functionalization approach for drugs, with a critical assessment of current literature and highlighting expected future progress and potential applications in the field.

CHEMICAL SOCIETY REVIEWS (2021)

Article Chemistry, Multidisciplinary

Nickel-Catalyzed Inter- and Intramolecular Aryl Thioether Metathesis by Reversible Arylation

Tristan Delcaillau et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2020)

Article Chemistry, Physical

Nickel-Catalyzed Amination of Aryl Thioethers: A Combined Synthetic and Mechanistic Study

Alessandro Bismuto et al.

ACS CATALYSIS (2020)

Article Chemistry, Multidisciplinary

Late-Stage Diversification of Natural Products

Benke Hong et al.

ACS CENTRAL SCIENCE (2020)

Article Chemistry, Multidisciplinary

Sulfonate Versus Sulfonate: Nickel and Palladium Multimetallic Cross-Electrophile Coupling of Aryl Triflates with Aryl Tosylates

Kai Kang et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2020)

Article Chemistry, Multidisciplinary

New Catalysis Concepts for Molecular Design and Feedstocks Valorization

Philip Boehm et al.

CHIMIA (2020)

Review Chemistry, Multidisciplinary

Catalytic Isofunctional Reactions-Expanding the Repertoire of Shuttle and Metathesis Reactions

Benjamin N. Bhawal et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2019)

Article Chemistry, Multidisciplinary

Alkenyl Exchange of Allylamines via Nickel(0)-Catalyzed C-C Bond Cleavage

Chao Fan et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2019)

Article Chemistry, Multidisciplinary

LiCl-Accelerated Multimetallic Cross-Coupling of Aryl Chlorides with Aryl Triflates

Liangbin Huang et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2019)

Review Chemistry, Multidisciplinary

Exploration of new reaction tools for late-stage functionalization of complex chemicals

Alejandra Dominguez-Huerta et al.

CANADIAN JOURNAL OF CHEMISTRY (2019)

Review Chemistry, Medicinal

Pharmaceutical and medicinal significance of sulfur (SVI)-Containing motifs for drug discovery: A critical review

Chuang Zhao et al.

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2019)

Article Chemistry, Multidisciplinary

Ni-Catalyzed Reductive Liebeskind-Srogl Alkylation of Heterocycles

Yuanhong Ma et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2019)

Article Chemistry, Multidisciplinary

Catalytic Transfer Hydration of Cyanohydrins to α-Hydroxyamides

Tomoya Kanda et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2019)

Article Chemistry, Multidisciplinary

Decarbonylative thioetherification by nickel catalysis using air- and moisture-stable nickel precatalysts

Chengwei Liu et al.

CHEMICAL COMMUNICATIONS (2018)

Article Chemistry, Multidisciplinary

Decarbonylative Aryl Thioether Synthesis by Ni Catalysis

Kota Ishitobi et al.

CHEMISTRY LETTERS (2018)

Article Chemistry, Organic

Decarbonylative Methylation of Aromatic Esters by a Nickel Catalyst

Toshimasa Okita et al.

ORGANIC LETTERS (2018)

Article Chemistry, Organic

Decarbonylative C-P Bond Formation Using Aromatic Esters and Organophosphorus Compounds

Ryota Isshiki et al.

ORGANIC LETTERS (2018)

Article Chemistry, Multidisciplinary

Functional Group Transposition: A Palladium-Catalyzed Metathesis of Ar-X σ-Bonds and Acid Chloride Synthesis

Maximiliano De La Higuera Macias et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2018)

Article Chemistry, Multidisciplinary

Decarbonylative Diaryl Ether Synthesis by Pd and Ni Catalysis

Ryosuke Takise et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2017)

Article Chemistry, Multidisciplinary

Visible-Light-Promoted C-S Cross-Coupling via Intermolecular Charge Transfer

Bin Liu et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2017)

Review Chemistry, Multidisciplinary

Cross-coupling of aromatic esters and amides

Ryosuke Takise et al.

CHEMICAL SOCIETY REVIEWS (2017)

Review Chemistry, Multidisciplinary

Enzymatic Carbon-Sulfur Bond Formation in Natural Product Biosynthesis

Kyle L. Dunbar et al.

CHEMICAL REVIEWS (2017)

Review Chemistry, Multidisciplinary

The medicinal chemist's toolbox for late stage functionalization of drug-like molecules

Tim Cernak et al.

CHEMICAL SOCIETY REVIEWS (2016)

Article Chemistry, Multidisciplinary

Photoredox Mediated Nickel Catalyzed Cross-Coupling of Thiols With Aryl and Heteroaryl Iodides via Thiyl Radicals

Martins S. Oderinde et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2016)

Article Chemistry, Organic

Cyanation of Phenol Derivatives with Aminoacetonitriles by Nickel Catalysis

Ryosuke Takise et al.

ORGANIC LETTERS (2016)

Article Chemistry, Multidisciplinary

Ni-Catalyzed α-arylation of esters and amides with phenol derivatives

Eva Koch et al.

CHEMICAL COMMUNICATIONS (2015)

Article Multidisciplinary Sciences

Multimetallic catalysed cross-coupling of aryl bromides with aryl triflates

Laura K. G. Ackerman et al.

NATURE (2015)

Article Multidisciplinary Sciences

Rh-catalyzed C-C bond cleavage by transfer hydroformylation

Stephen K. Murphy et al.

SCIENCE (2015)

Article Chemistry, Multidisciplinary

Nickel-Catalyzed α-Arylation of Ketones with Phenol Derivatives

Ryosuke Takise et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2014)

Article Chemistry, Multidisciplinary

Palladium-Catalyzed Amination of Aryl Sulfides with Anilines

Tomohiro Sugahara et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2014)

Article Chemistry, Multidisciplinary

A Mild, One-Pot Stadler-Ziegler Synthesis of Arylsulfides Facilitated by Photoredox Catalysis in Batch and Continuous-Flow

Xiao Wang et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2013)

Review Chemistry, Multidisciplinary

Transition-metal mediated carbon-sulfur bond activation and transformations

Liandi Wang et al.

CHEMICAL SOCIETY REVIEWS (2013)

Review Chemistry, Multidisciplinary

Transition metal-catalyzed C-C bond formation via C-S bond cleavage: an overview

Sachin G. Modha et al.

CHEMICAL SOCIETY REVIEWS (2013)

Article Chemistry, Organic

Ligand-Free Ni-Catalyzed Reductive Cleavage of Inert Carbon-Sulfur Bonds

Nekane Barbero et al.

ORGANIC LETTERS (2012)

Article Chemistry, Multidisciplinary

Carbon-Sulfur Bond Formation of Challenging Substrates at Low Temperature by Using Pd-PEPPSI-IPent

Mahmoud Sayah et al.

CHEMISTRY-A EUROPEAN JOURNAL (2011)

Article Chemistry, Organic

Equilibrium shift in the rhodium-catalyzed acyl transfer reactions

Mieko Arisawa et al.

TETRAHEDRON (2011)

Article Chemistry, Multidisciplinary

Resting State and Elementary Steps of the Coupling of Aryl Halides with Thiols Catalyzed by Alkylbisphosphine Complexes of Palladium

Elsa Alvaro et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2009)

Article Chemistry, Multidisciplinary

A general and long-lived catalyst for the palladium-catalyzed coupling of aryl halides with thiols

MA Fernández-Rodríguez et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2006)

Review Chemistry, Multidisciplinary

Organosulfur compounds: Electrophilic reagents in transition-metal-catalyzed carbon-carbon bond-forming reactions

SR Dubbaka et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2005)

Review Chemistry, Multidisciplinary

Modern synthetic methods for copper-mediated C(aryl)-O, C(aryl)-N, and C(aryl)-S bond formation

SV Ley et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2003)

Review Chemistry, Multidisciplinary

Metal-catalyzed carbon-sulfur bond formation

T Kondo et al.

CHEMICAL REVIEWS (2000)