efficient buchwald hartwig reaction catalyzed by spions-bis(nhc)-pd(ii)
Authors
abstract
a powerful and convenient reaction procedure for the c-n coupling reaction (the buchwald-hartwig reaction), yielding products of n-arylanilines and n-arylamines in both conventional heating and microwave irradiation has been reported. the protocol utilizes a stable and new supper ferromagnetic nanoparticle chelating n-heterocyclic dicarbene palladium(ii) complex (pd-nhc) as catalyst which helps/allows us to complete the reaction with only 0.002 mol% pd producing high yield products. we also examined the reusability of the catalyst. it was found that the catalyst could be recovered by external magnetic field and reused for seven times without obvious loss in catalytic activity.
similar resources
Efficient buchwald hartwig reaction catalyzed by spions-bis(NHC)-Pd(II)
A powerful and convenient reaction procedure for the C-N coupling reaction (the Buchwald-Hartwig reaction), yielding products of N-arylanilines and N-arylamines in both conventional heating and microwave irradiation has been reported. The protocol utilizes a stable and new supper ferromagnetic nanoparticle chelating N-heterocyclic dicarbene palladium(II) complex (Pd-NHC) as catalyst which helps...
full textSynthesis of Symmetrical Triaryl Amines by Nano-CuO Catalyzed Buchwald-Hartwig Cross-coupling Reaction: NH2-Thiadiazole as a New N-source
The one-pot synthesis of symmetrical triaryl amines using aryl halides and 5-Methyl-1,3,4-Thiadiazole-2-Amine as a nitrogen-transfer reagent is reported. Copper oxide nanoparticles that does not require the presence of any additional ligand, improved rate and facility of the synthesis of triaryl amines. The introduction of a new N-source, using green solvents PEG/H2O, normal atmospheric conditi...
full textConstruction of tetrahydrofurans by PdII/PdIV-catalyzed aminooxygenation of alkenes.
Catalytic transformations involving Pd s-alkyl or s-aryl intermediates are widely used in organic synthesis and offer attractive routes to many valuable products. However, the vast majority of these reactions proceed by Pd/Pd mechanisms. As a result, the diversity of structures/bonds that can be constructed is constrained by the limitations of this redox cycle. Recent studies have explored the ...
full textSynthesis of 7-aminocoumarin by Buchwald-Hartwig cross coupling for specific protein labeling in living cells.
The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters. To enable minimally invasive studies of proteins in their native context, it is desirable to tag proteins with small, bright reporter groups. Recently, our lab described PRIME technology (for PRobe Incorporation Mediated by Enzymes) for such tagging [1-3]. An engineered variant...
full textSynthesis of 7-aminocoumarin via Buchwald-Hartwig cross coupling for specific protein labeling in living cells
The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters. To enable minimally invasive studies of proteins in their native context, it is desirable to tag proteins with small, bright reporter groups. Recently, our lab described PRIME technology (for PRobe Incorporation Mediated by Enzymes) for such tagging [1-3]. An engineered variant...
full textThe Evolution of Pd0/PdII-Catalyzed Aromatic Fluorination
Aromatic fluorides are prevalent in both agrochemical and pharmaceutical agents. However, methods for their rapid and general preparation from widely available starting materials are limited. Traditional approaches such as the Balz-Schiemann and Halex reactions require harsh conditions that limit functional group tolerance and substrate scope. The use of transition metals to affect C-F bond for...
full textMy Resources
Save resource for easier access later
Journal title:
nanochemistry researchPublisher: iranian chemical society
ISSN 2423-818X
volume 1
issue 1 2016
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023