Literature DB >> 22384311

Palladium-Catalyzed Coupling of Functionalized Primary and Secondary Amines with Aryl and Heteroaryl Halides: Two Ligands Suffice in Most Cases.

Debabrata Maiti1, Brett P Fors, Jaclyn L Henderson, Yoshinori Nakamura, Stephen L Buchwald.   

Abstract

We report our studies on the use of two catalyst systems, based on the ligands BrettPhos (1) and RuPhos (2), which provide the widest scope for Pd-catalyzed C-N cross-coupling reactions to date. Often low catalyst loadings and short reaction times can be used with functionalized aryl and heteroaryl coupling partners. The reactions are highly robust and can be set up and performed without the use of a glovebox. These catalysts should find wide application in the synthesis of complex molecules including pharmaceuticals, natural products and functional materials.

Entities:  

Year:  2011        PMID: 22384311      PMCID: PMC3289414          DOI: 10.1039/C0SC00330A

Source DB:  PubMed          Journal:  Chem Sci        ISSN: 2041-6520            Impact factor:   9.825


  45 in total

1.  Improved functional group compatibility in the palladium-catalyzed synthesis of aryl amines.

Authors:  Michele C Harris; Xiaohua Huang; Stephen L Buchwald
Journal:  Org Lett       Date:  2002-08-22       Impact factor: 6.005

2.  Amino acid promoted CuI-catalyzed C-N bond formation between aryl halides and amines or N-containing heterocycles.

Authors:  Hui Zhang; Qian Cai; Dawei Ma
Journal:  J Org Chem       Date:  2005-06-24       Impact factor: 4.354

Review 3.  Palladium complexes of N-heterocyclic carbenes as catalysts for cross-coupling reactions--a synthetic chemist's perspective.

Authors:  Eric Assen B Kantchev; Christopher J O'Brien; Michael G Organ
Journal:  Angew Chem Int Ed Engl       Date:  2007       Impact factor: 15.336

4.  Hole-transporting hydrazones.

Authors:  Ramūnas Lygaitis; Vytautas Getautis; Juozas Vidas Grazulevicius
Journal:  Chem Soc Rev       Date:  2008-02-15       Impact factor: 54.564

5.  Synthesis of C8-adenosine adducts of arylamines using palladium catalysis.

Authors:  E Schoffers; P D Olsen; J C Means
Journal:  Org Lett       Date:  2001-12-27       Impact factor: 6.005

6.  Copper/amino acid catalyzed cross-couplings of aryl and vinyl halides with nucleophiles.

Authors:  Dawei Ma; Qian Cai
Journal:  Acc Chem Res       Date:  2008-11-18       Impact factor: 22.384

7.  Evolution of a fourth generation catalyst for the amination and thioetherification of aryl halides.

Authors:  John F Hartwig
Journal:  Acc Chem Res       Date:  2008-11-18       Impact factor: 22.384

8.  Development of CXCR3 antagonists. Part 4: discovery of 2-amino-(4-tropinyl)quinolines.

Authors:  Roland L Knight; Daniel R Allen; Helen L Birch; Gayle A Chapman; Frances C Galvin; Louise A Jopling; Christopher J Lock; Johannes W G Meissner; David A Owen; Gilles Raphy; Robert J Watson; Sophie C Williams
Journal:  Bioorg Med Chem Lett       Date:  2007-11-28       Impact factor: 2.823

9.  Discovery and characterization of 4'-(2-furyl)-N-pyridin-3-yl-4,5'-bipyrimidin-2'-amine (LAS38096), a potent, selective, and efficacious A2B adenosine receptor antagonist.

Authors:  Bernat Vidal; Arsenio Nueda; Cristina Esteve; Teresa Domenech; Sonia Benito; Raquel F Reinoso; Mercè Pont; Marta Calbet; Rosa López; María Isabel Cadavid; María Isabel Loza; Alvaro Cárdenas; Núria Godessart; Jorge Beleta; Graham Warrellow; Hamish Ryder
Journal:  J Med Chem       Date:  2007-05-01       Impact factor: 7.446

10.  An efficient process for pd-catalyzed C-N cross-coupling reactions of aryl iodides: insight into controlling factors.

Authors:  Brett P Fors; Nicole R Davis; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2009-04-29       Impact factor: 15.419

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  35 in total

1.  Late-Stage Diversification of Biologically Active Molecules via Chemoenzymatic C-H Functionalization.

Authors:  Landon J Durak; James T Payne; Jared C Lewis
Journal:  ACS Catal       Date:  2016-01-25       Impact factor: 13.084

2.  Design of New Ligands for the Palladium-Catalyzed Arylation of α-Branched Secondary Amines.

Authors:  Nathaniel H Park; Ekaterina V Vinogradova; David S Surry; Stephen L Buchwald
Journal:  Angew Chem Int Ed Engl       Date:  2015-06-01       Impact factor: 15.336

3.  A bulky biaryl phosphine ligand allows for palladium-catalyzed amidation of five-membered heterocycles as electrophiles.

Authors:  Mingjuan Su; Stephen L Buchwald
Journal:  Angew Chem Int Ed Engl       Date:  2012-03-30       Impact factor: 15.336

4.  Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide.

Authors:  David S Surry; Stephen L Buchwald
Journal:  Chem Sci       Date:  2011       Impact factor: 9.825

5.  Electrochemically Enabled, Nickel-Catalyzed Amination.

Authors:  Chao Li; Yu Kawamata; Hugh Nakamura; Julien C Vantourout; Zhiqing Liu; Qinglong Hou; Denghui Bao; Jeremy T Starr; Jinshan Chen; Ming Yan; Phil S Baran
Journal:  Angew Chem Int Ed Engl       Date:  2017-09-14       Impact factor: 15.336

6.  Palladium-catalyzed N-arylation of 2-aminothiazoles.

Authors:  Meredeth A McGowan; Jaclyn L Henderson; Stephen L Buchwald
Journal:  Org Lett       Date:  2012-03-06       Impact factor: 6.005

7.  Enantioselective total syntheses of plectosphaeroic acids B and C.

Authors:  Salman Y Jabri; Larry E Overman
Journal:  J Org Chem       Date:  2013-08-27       Impact factor: 4.354

8.  Pd-Catalyzed Decarbonylative Cross-Couplings of Aroyl Chlorides.

Authors:  Christian A Malapit; Naoko Ichiishi; Melanie S Sanford
Journal:  Org Lett       Date:  2017-07-19       Impact factor: 6.005

9.  An Improved Synthesis of BrettPhos and RockPhos-Type Biarylphosphine Ligands.

Authors:  Naoyuki Hoshiya; Stephen L Buchwald
Journal:  Adv Synth Catal       Date:  2012-06-27       Impact factor: 5.837

10.  The structure-activity relationships of L3MBTL3 inhibitors: flexibility of the dimer interface.

Authors:  Michelle A Camerino; Nan Zhong; Aiping Dong; Bradley M Dickson; Lindsey I James; Brandi M Baughman; Jacqueline L Norris; Dmitri B Kireev; William P Janzen; Cheryl H Arrowsmith; Stephen V Frye
Journal:  Medchemcomm       Date:  2013-11       Impact factor: 3.597

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