4.7 Article

Catalyst-free, radical-mediated intermolecular 1,2-arylheteroarylation of alkenes by cleaving inert C-C bond

Related references

Note: Only part of the references are listed.
Article Chemistry, Multidisciplinary

Electrochemical 1,2-Diarylation of Alkenes Enabled by Direct Dual C-H Functionalizations of Electron-Rich Aromatic Hydrocarbons

Jing-Hao Qin et al.

Summary: This study describes a cobalt-promoted electrochemical method for 1,2-diarylation of alkenes with electron-rich aromatic hydrocarbons, producing polyaryl-functionalized alkanes. Utilizing a radical relay strategy, the chemoselectivity is shifted to dehydrogenative [2+2+2] cycloaddition via 1,2-diarylation by using a graphite rod cathode, resulting in the formation of complex 11,12-dihydroindolo[2,3-a]carbazoles.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2021)

Review Chemistry, Multidisciplinary

Synthetic Applications of Oxidative Aromatic Coupling-From Biphenols to Nanographenes

Marek Grzybowski et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2020)

Article Chemistry, Multidisciplinary

Gold-Catalyzed 1,2-Diarylation of Alkenes

Chetan C. Chintawar et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2020)

Review Chemistry, Multidisciplinary

Radical-Mediated Remote Functional Group Migration

Xinxin Wu et al.

ACCOUNTS OF CHEMICAL RESEARCH (2020)

Article Chemistry, Multidisciplinary

Nickel-Catalyzed Asymmetric Reductive Diarylation of Vinylarenes

David Anthony et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2019)

Article Chemistry, Multidisciplinary

Three-component vicinal-diarylation of alkenes via direct transmetalation of arylboronic acids

Yun Zhang et al.

CHEMICAL SCIENCE (2019)

Article Chemistry, Multidisciplinary

Tertiary-Alcohol-Directed Functionalization of Remote C(sp(3))-H Bonds by Sequential Hydrogen Atom and Heteroaryl Migrations

Xinxin Wu et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2018)

Article Chemistry, Multidisciplinary

1,2-Diarylation of alkenes with aryldiazonium salts and arenes enabled by visible light photoredox catalysis

Xuan-Hui Ouyang et al.

CHEMICAL COMMUNICATIONS (2018)

Article Chemistry, Multidisciplinary

Nickel-Catalyzed Stereoselective Diarylation of Alkenylarenes

Pin Gao et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2018)

Article Chemistry, Multidisciplinary

Ni-Catalyzed Enantioselective Reductive Diarylation of Activated Alkenes by Domino Cyclization/Cross-Coupling

Kuai Wang et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2018)

Article Chemistry, Multidisciplinary

Nickel-Catalyzed 1,2-Diarylation of Simple Alkenyl Amides

Joseph Derosa et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2018)

Review Chemistry, Medicinal

Indole-fused azepines and analogues as anticancer lead molecules: Privileged findings and future directions

Ashok K. Singh et al.

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2017)

Article Chemistry, Multidisciplinary

Nickel-Catalyzed β,γ-Dicarbofunctionalization of Alkenyl Carbonyl Compounds via Conjunctive Cross-Coupling

Joseph Derosa et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2017)

Article Chemistry, Multidisciplinary

Chemo- and Regioselective Distal Heteroaryl ipso-Migration: A General Protocol for Heteroarylation of Unactivated Alkenes

Zhen Wu et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2017)

Article Chemistry, Organic

Pd-Catalyzed 1,2-diarylation of vinylarenes at ambient temperature

Zhijie Kuang et al.

ORGANIC CHEMISTRY FRONTIERS (2017)

Review Chemistry, Multidisciplinary

Catalysis of Radical Reactions: A Radical Chemistry Perspective

Armido Studer et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2016)

Article Chemistry, Multidisciplinary

Radical Hydrodeiodination of Aryl, Alkenyl, Alkynyl, and Alkyl Iodides with an Alcoholate as Organic Chain Reductant through Electron Catalysis

Abhishek Dewanji et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2016)

Article Chemistry, Multidisciplinary

Reductive Cross-Coupling of Conjugated Arylalkenes and Aryl Bromides with Hydrosilanes by Cooperative Palladium/Copper Catalysis

Kazuhiko Semba et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2016)

Article Chemistry, Multidisciplinary

β,γ-Vicinal Dicarbofunctionalization of Alkenyl Carbonyl Compounds via Directed Nucleopalladation

Zhen Liu et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2016)

Article Chemistry, Multidisciplinary

Diarylation of Alkenes by a Cu-Catalyzed Migratory Insertion/Cross-Coupling Cascade

Wei You et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2014)

Review Chemistry, Multidisciplinary

The electron is a catalyst

Armido Studer et al.

NATURE CHEMISTRY (2014)

Article Chemistry, Multidisciplinary

Borontribromide-mediated C-C bond formation in cyclic ketones: a transition metal free approach

Imran Ahmad et al.

RSC ADVANCES (2014)

Article Chemistry, Organic

Pd(0)-Catalyzed 1,1-Diarylation of Ethylene and Allylic Carbonates

Vaneet Saini et al.

ORGANIC LETTERS (2013)

Article Chemistry, Multidisciplinary

Synthesis of Enantioenriched Triarylmethanes by Stereospecific Cross-Coupling Reactions

Buck L. H. Taylor et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2012)

Article Chemistry, Organic

Asymmetric palladium-catalyzed hydroarylation of styrenes and dienes

Susanne M. Podhajsky et al.

TETRAHEDRON (2011)

Article Chemistry, Multidisciplinary

Palladium-Catalyzed Oxidative Intermolecular Difunctionalization of Terminal Alkenes with Organostannanes and Molecular Oxygen

Kaveri Balan Urkalan et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2009)

Article Chemistry, Multidisciplinary

Aerobic alcohol oxidation coupled to palladium-catalyzed alkene hydroarylation with boronic esters

Yasumasa Iwai et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2008)

Article Chemistry, Multidisciplinary

Palladium-catalyzed reductive coupling of styrenes and organostannanes under aerobic conditions

Keith M. Gligorich et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2007)

Article Biochemistry & Molecular Biology

Design and synthesis of 3-phenyl tetrahydronaphthalenic derivatives as new selective MT2 melatoninergic ligands

S Yous et al.

BIOORGANIC & MEDICINAL CHEMISTRY (2003)