Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Klára Aradi"'
Publikováno v:
Results in Chemistry, Vol 7, Iss , Pp 101309- (2024)
A study on some halofluorination and fluoroselenation protocols of various functionalized cyclic olefins, such as esters, lactams or amino esters as model compounds is presented. The ring olefin bond functionalizations were based on their activation
Externí odkaz:
https://doaj.org/article/b4fd2726e9904c4b8b41c6cd7597900e
Autor:
Loránd Kiss, Klára Aradi
Publikováno v:
Synthesis. 55:1834-1843
Due to the increasing need for fluorine-containing drugs, the synthesis of organofluorine scaffolds has become a highly researched area of synthetic organic chemistry. The introduction of the trifluoromethyl group into the structure of an organic mol
Autor:
Klára Aradi, Loránd Kiss
Publikováno v:
Chemistry – A European Journal. 29
Autor:
Klára Aradi, Loránd Kiss
Publikováno v:
Chemistry – A European Journal. 29
Organofluorine chemistry has become an expanding area of research in organic chemistry and drug design. The synthesis of fluorine-containing molecules has received high significance in synthetic chemistry. Trifluoromethylative difunctionalizations of
Publikováno v:
Synlett. 27:1456-1485
This account aims to give a description of the usefulness of diaryliodonium salts in organic chemistry, including their synthesis and applications in the presence and absence of transition-metal catalysts. Herein, we briefly summarize the structural
Publikováno v:
The Journal of Organic Chemistry. 81:920-931
A novel, highly modular synthetic method with high functional group tolerance was developed for the construction of chromenoquinoline derivatives from arylpropynyloxy-benzonitriles and diaryliodonium triflates via an oxidative arylation-cyclization p
Autor:
Zoltán Novák, Klára Aradi
Publikováno v:
Advanced Synthesis & Catalysis. 357:371-376
A novel, highly modular synthetic methodology with high functional group tolerance is developed for the construction of iminobenzoxazine derivatives from ortho-cyanoanilides and diaryliodonium triflates via an oxidative arylation—cyclization path.
Publikováno v:
The Journal of organic chemistry. 82(22)
A novel synthetic methodology was developed for the N-arylation of nitroenamine derivatives utilizing diaryliodonium triflates and copper(I) chloride as a catalyst. The procedure enables the easy aryl transfer from the hypervalent species under mild
Publikováno v:
Organic letters. 19(4)
A novel catalytic method for the direct C–H alkynylation of azulenes is developed. The gold catalyzed functionalization of this special carbacycle is achieved with hypervalent iodonium reagent TIPS-EBX under mild reaction conditions. With the aid o
Publikováno v:
ChemInform. 47
This account aims to give a description of the usefulness of diaryliodonium salts in organic chemistry, including their synthesis and applications in the presence and absence of transition-metal catalysts. Herein, we briefly summarize the structural