-
Something wrong with this record ?
New Stable Cu(I) Catalyst Supported on Weakly Acidic Polyacrylate Resin for Green C-N Coupling: Synthesis of N-(Pyridin-4-yl)benzene Amines and N,N-Bis(pyridine-4-yl)benzene Amines
N. Kore, P. Pazdera,
Language English Country Switzerland
Document type Journal Article
NLK
Directory of Open Access Journals
from 1997
Free Medical Journals
from 1997
PubMed Central
from 2001
Europe PubMed Central
from 2001
ProQuest Central
from 1997-01-01
Open Access Digital Library
from 1997-01-01
Medline Complete (EBSCOhost)
from 2009-03-01
Health & Medicine (ProQuest)
from 1997-01-01
- MeSH
- 2-Naphthylamine chemistry MeSH
- Acrylic Resins chemistry MeSH
- Aniline Compounds chemistry MeSH
- Electrons * MeSH
- Catalysis MeSH
- Hydrogen-Ion Concentration MeSH
- Copper chemistry MeSH
- Equipment Reuse MeSH
- Piperazines chemistry MeSH
- Pyridinium Compounds chemical synthesis MeSH
- Green Chemistry Technology MeSH
- Publication type
- Journal Article MeSH
A method for preparation of a new stable Cu(I) catalyst supported on weakly acidic polyacrylate resin without additional stabilizing ligands is described. A simple and efficient methodology for Ullmann Cu(I) catalyzed C-N cross coupling reactions using this original catalyst is reported. Coupling reactions of 4-chloropyridinium chloride with anilines containing electron donating (EDG) or electron withdrawing (EWG) groups, naphthalen-2-amine and piperazine, respectively, are successfully demonstrated.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17023403
- 003
- CZ-PrNML
- 005
- 20170720124151.0
- 007
- ta
- 008
- 170720s2016 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/molecules22010002 $2 doi
- 035 __
- $a (PubMed)28025513
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Kore, Nitin $u Centre for Syntheses at Sustainable Conditions and their Management, Department of Chemistry, Faculty of Science, Masaryk University, Kamenice 5, CZ-62500 Brno, Czech Republic. kore_ns@yahoo.co.in.
- 245 10
- $a New Stable Cu(I) Catalyst Supported on Weakly Acidic Polyacrylate Resin for Green C-N Coupling: Synthesis of N-(Pyridin-4-yl)benzene Amines and N,N-Bis(pyridine-4-yl)benzene Amines / $c N. Kore, P. Pazdera,
- 520 9_
- $a A method for preparation of a new stable Cu(I) catalyst supported on weakly acidic polyacrylate resin without additional stabilizing ligands is described. A simple and efficient methodology for Ullmann Cu(I) catalyzed C-N cross coupling reactions using this original catalyst is reported. Coupling reactions of 4-chloropyridinium chloride with anilines containing electron donating (EDG) or electron withdrawing (EWG) groups, naphthalen-2-amine and piperazine, respectively, are successfully demonstrated.
- 650 _2
- $a 2-naftylamin $x chemie $7 D015081
- 650 _2
- $a akrylové pryskyřice $x chemie $7 D000180
- 650 _2
- $a aniliny $x chemie $7 D000814
- 650 _2
- $a katalýza $7 D002384
- 650 _2
- $a měď $x chemie $7 D003300
- 650 12
- $a elektrony $7 D004583
- 650 _2
- $a opakované použití vybavení $7 D017743
- 650 _2
- $a technologie zelené chemie $7 D055772
- 650 _2
- $a koncentrace vodíkových iontů $7 D006863
- 650 _2
- $a piperaziny $x chemie $7 D010879
- 650 _2
- $a pyridinové sloučeniny $x chemická syntéza $7 D011726
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Pazdera, Pavel $u Centre for Syntheses at Sustainable Conditions and their Management, Department of Chemistry, Faculty of Science, Masaryk University, Kamenice 5, CZ-62500 Brno, Czech Republic. pazdera@chemi.muni.cz.
- 773 0_
- $w MED00180394 $t Molecules (Basel, Switzerland) $x 1420-3049 $g Roč. 22, č. 1 (2016)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/28025513 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20170720 $b ABA008
- 991 __
- $a 20170720124644 $b ABA008
- 999 __
- $a ok $b bmc $g 1239084 $s 984316
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2016 $b 22 $c 1 $e 20161222 $i 1420-3049 $m Molecules $n Molecules $x MED00180394
- LZP __
- $a Pubmed-20170720
