Literature DB >> 15104459

Cross-coupling and dehalogenation reactions catalyzed by (N-heterocyclic carbene)Pd(allyl)Cl complexes.

Oscar Navarro1, Harneet Kaur, Parisa Mahjoor, Steven P Nolan.   

Abstract

A series of well-defined, air- and moisture-stable (NHC)Pd(allyl)Cl (NHC = N-heterocyclic carbene) complexes has been used in several catalytic reactions: Suzuki-Miyaura cross-coupling, catalytic dehalogenation of aryl halides, and aryl amination. The scope of the three processes using various substrates was examined. A general system involving the use of (IPr)Pd(allyl)Cl as catalyst and NaO(t)Bu as base has proven to be highly active for the Suzuki-Miyaura cross-coupling of activated and unactivated aryl chlorides and bromides, for the catalytic dehalogenation of aryl chlorides, and for the catalytic aryl amination of aryl triflates. All reactions proceed in short reaction times and at mild temperatures. The system has also proven to be compatible with the microwave-assisted Suzuki-Miyaura cross-coupling and catalytic dehalogenation processes, affording yields similar to those of the conventionally heated analogous reactions.

Entities:  

Year:  2004        PMID: 15104459     DOI: 10.1021/jo035834p

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  17 in total

1.  Reductions of aryl bromides in water at room temperature.

Authors:  James C Fennewald; Evan B Landstrom; Bruce H Lipshutz
Journal:  Tetrahedron Lett       Date:  2015-06-03       Impact factor: 2.415

Review 2.  Controlled microwave heating in modern organic synthesis: highlights from the 2004-2008 literature.

Authors:  C Oliver Kappe; Doris Dallinger
Journal:  Mol Divers       Date:  2009-04-21       Impact factor: 2.943

3.  Cross-Coupling and Related Reactions: Connecting Past Success to the Development of New Reactions for the Future.

Authors:  Louis-Charles Campeau; Nilay Hazari
Journal:  Organometallics       Date:  2018-11-27       Impact factor: 3.876

4.  Differences in the Performance of Allyl Based Palladium Precatalysts for Suzuki-Miyaura Reactions.

Authors:  Matthew R Espinosa; Angelino Doppiu; Nilay Hazari
Journal:  Adv Synth Catal       Date:  2020-08-27       Impact factor: 5.837

5.  Studies of microwave-enhanced Suzuki-Miyaura vinylation of electron-rich sterically hindered substrates utilizing potassium vinyltrifluoroborate.

Authors:  Matthew D Brooker; Stefan M Cooper; Dena R Hodges; Rhiannon R Carter; Justin K Wyatt
Journal:  Tetrahedron Lett       Date:  2010-12-22       Impact factor: 2.415

6.  Bis{1-[2-(diphenyl-phosphino)-ethyl]-3-ethylimidazol-2-yl-idene}palladium(II) bis-(hexa-fluoridophosphate) acetonitrile 2.85-solvate.

Authors:  A Ahmida Aziza; Ulrich Flörke; Hans Egold; Gerald Henkel
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-04-14

7.  Effects of Bases and Halides on the Amination of Chloroarenes Catalyzed by Pd(PtBu3)2.

Authors:  Shashank Shekhar; John F Hartwig
Journal:  Organometallics       Date:  2006-12-19       Impact factor: 3.876

8.  Air-stable, recyclable, and time-efficient diphenylphosphinite cellulose-supported palladium nanoparticles as a catalyst for Suzuki-Miyaura reactions.

Authors:  Qingwei Du; Yiqun Li
Journal:  Beilstein J Org Chem       Date:  2011-03-30       Impact factor: 2.883

9.  Synthesis of chiral mono(N-heterocyclic carbene) palladium and gold complexes with a 1,1'-biphenyl scaffold and their applications in catalysis.

Authors:  Lian-Jun Liu; Feijun Wang; Wenfeng Wang; Mei-Xin Zhao; Min Shi
Journal:  Beilstein J Org Chem       Date:  2011-05-04       Impact factor: 2.883

10.  Modular assembly of a Pd catalyst within a DNA scaffold for the amplified colorimetric and fluorimetric detection of nucleic acids.

Authors:  Deepak K Prusty; Minseok Kwak; Jur Wildeman; Andreas Herrmann
Journal:  Angew Chem Int Ed Engl       Date:  2012-10-17       Impact factor: 15.336

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