Literature DB >> 21506178

Recent progress in coupling of two heteroarenes.

Dongbing Zhao1, Jingsong You, Changwei Hu.   

Abstract

The biheteroaryl structural motif is prevalent in polymers, advanced materials, liquid crystals, ligands, molecules of medicinal interest, and natural products. Many types of synthetic transformations have been known for the construction of heteroaryl-heteroaryl linkages. Coupling reactions provide one of the most efficient ways to achieve these biheterocyclic structures. In this review, four types of coupling reactions are discussed: 1) transition-metal-catalyzed coupling reactions of heteroaryl halides or surrogates with heteroarylmetals; 2) direct inter- and intramolecular heteroarylations of C sp 2-H bonds of heteroarenes with heteroaryl halides or pseudohalides; 3) oxidative C-H/C-H homo- and cross-couplings of two unpreactivated heteroarenes; and 4) transition-metal-catalyzed decarboxylative cross-coupling reactions between haloheteroarenes or heteroarenes and heteroarenecarboxylic acids. The general purpose of this review is to give an exhaustive and clear picture in heteroaryl-heteroaryl bond formation as well as its application in the synthesis of natural products, pharmaceuticals, catalyst ligands, and materials.
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2011        PMID: 21506178     DOI: 10.1002/chem.201003039

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  11 in total

1.  Heterobiaryl synthesis by contractive C-C coupling via P(V) intermediates.

Authors:  Michael C Hilton; Xuan Zhang; Benjamin T Boyle; Juan V Alegre-Requena; Robert S Paton; Andrew McNally
Journal:  Science       Date:  2018-11-16       Impact factor: 47.728

2.  A General, Multimetallic Cross-Ullmann Biheteroaryl Synthesis from Heteroaryl Halides and Heteroaryl Triflates.

Authors:  Kai Kang; Nathan L Loud; Tarah A DiBenedetto; Daniel J Weix
Journal:  J Am Chem Soc       Date:  2021-12-17       Impact factor: 15.419

3.  Nickel-catalyzed Suzuki-Miyaura couplings in green solvents.

Authors:  Stephen D Ramgren; Liana Hie; Yuxuan Ye; Neil K Garg
Journal:  Org Lett       Date:  2013-07-23       Impact factor: 6.005

4.  Palladium-catalyzed direct C-H arylation of cyclic enaminones with aryl iodides.

Authors:  Yi-Yun Yu; Lei Bi; Gunda I Georg
Journal:  J Org Chem       Date:  2013-06-10       Impact factor: 4.354

5.  Indolizines and pyrrolo[1,2-c]pyrimidines decorated with a pyrimidine and a pyridine unit respectively.

Authors:  Marcel Mirel Popa; Emilian Georgescu; Mino R Caira; Florentina Georgescu; Constantin Draghici; Raluca Stan; Calin Deleanu; Florea Dumitrascu
Journal:  Beilstein J Org Chem       Date:  2015-06-26       Impact factor: 2.883

6.  Ru-catalysed C-H arylation of indoles and pyrroles with boronic acids: scope and mechanistic studies.

Authors:  Carina Sollert; Karthik Devaraj; Andreas Orthaber; Paul J Gates; Lukasz T Pilarski
Journal:  Chemistry       Date:  2015-02-17       Impact factor: 5.236

7.  Direct arylation catalysis with chloro[8-(dimesitylboryl)quinoline-κN]copper(I).

Authors:  Sem Raj Tamang; James D Hoefelmeyer
Journal:  Beilstein J Org Chem       Date:  2016-12-15       Impact factor: 2.883

8.  Rhodium-catalyzed ortho-heteroarylation of phenols: directing group-enabled switching of the electronic bias for heteroaromatic coupling partner.

Authors:  Yimin Wu; Wei Li; Linfeng Jiang; Luoqiang Zhang; Jingbo Lan; Jingsong You
Journal:  Chem Sci       Date:  2018-07-18       Impact factor: 9.825

9.  Copper-catalyzed CuAAC/intramolecular C-H arylation sequence: Synthesis of annulated 1,2,3-triazoles.

Authors:  Rajkumar Jeyachandran; Harish Kumar Potukuchi; Lutz Ackermann
Journal:  Beilstein J Org Chem       Date:  2012-10-16       Impact factor: 2.883

10.  Palladium-catalyzed difluoromethylthiolation of heteroaryl bromides, iodides, triflates and aryl iodides.

Authors:  Jiang Wu; Yafei Liu; Changhui Lu; Qilong Shen
Journal:  Chem Sci       Date:  2016-02-17       Impact factor: 9.825

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