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Barbara Balázs

Bio: Barbara Balázs is an academic researcher from Hungarian Academy of Sciences. The author has contributed to research in topics: Nitrile & Cycloaddition. The author has an hindex of 9, co-authored 27 publications receiving 262 citations. Previous affiliations of Barbara Balázs include Szent István University & Budapest University of Technology and Economics.

Papers
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Journal ArticleDOI
TL;DR: In this paper, the conformation of calix(aza)crowns has been investigated and comprehensive NMR investigations have been made to reveal the conformities of the crowns 2, 3, 4.

61 citations

Journal ArticleDOI
TL;DR: Inherently chiral calix[4]arenes with carboxamide bridges spanning the proximal positions on the lower rim and 18 achiral counterparts have been synthesized by double intramolecular cyclization of 7b,8b 1,3-and 17 1,2-bis-chloroalkylamides as mentioned in this paper.

42 citations

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TL;DR: The endo/exo quinoid tautomerism of the chromophore and the mechanism of the coloration process were studied by NMR spectroscopy as discussed by the authors.

24 citations

Journal ArticleDOI
TL;DR: In this article, the regio-and stereoselective synthesis of spiropyrazolines 7 and 8 via 1,3-dipolar cycloaddition of C-2-(5-nitrofuryl)-N-methylnitrilimine, C- 2-(5,nitro-fury l)N-phenylnitrinimine and C-4-nitrophenyl-N-mmethyl-nitrilinimine to (E)-3-benzylidenechromanone (1), -

21 citations

Journal ArticleDOI
TL;DR: In this article, the binding sites of the target molecules performed in various solvents in the presence of weak base and alkali cations revealed Li+, Na+ and Ca2+ recognition depending on their binding sites.

18 citations


Cited by
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Journal ArticleDOI
26 Jul 2019-Science
TL;DR: A stable organic semiconductor material, mesoporous graphitic carbon nitride (mpg-CN), can act as a visible-light photoredox catalyst to orchestrate oxidative and reductive interfacial electron transfers to two different substrates in a two- or three-component system for direct twofold carbon–hydrogen functionalization of arenes and heteroarenes.
Abstract: Photoexcited electron-hole pairs on a semiconductor surface can engage in redox reactions with two different substrates. Similar to conventional electrosynthesis, the primary redox intermediates afford only separate oxidized and reduced products or, more rarely, combine to one addition product. Here, we report that a stable organic semiconductor material, mesoporous graphitic carbon nitride (mpg-CN), can act as a visible-light photoredox catalyst to orchestrate oxidative and reductive interfacial electron transfers to two different substrates in a two- or three-component system for direct twofold carbon-hydrogen functionalization of arenes and heteroarenes. The mpg-CN catalyst tolerates reactive radicals and strong nucleophiles, is straightforwardly recoverable by simple centrifugation of reaction mixtures, and is reusable for at least four catalytic transformations with conserved activity.

348 citations

Journal ArticleDOI
TL;DR: The aim of this review is to summarize the various naturally occurring chalcone compounds which have been isolated from different plants to initiate further pharmacobotanical, biotechnological and medicinal studies on the field of chal cone research.
Abstract: The aim of this review is to summarize the various naturally occurring chalcone compounds which have been isolated from different plants. Chalcones considered as obligate intermediated in flavonoid biosynthesis but they do not accumulate to appreciable degree in most plants. The largest number of natural chalcones has been isolated from species of the Leguminosae, Asteraceae and Moraceae families. Chalcone accumulating plants have often been used in traditional medicine and chalcones have therefore been studied and reported to possess many beneficial biological effects including anti-inflammatory, antimicrobial, antifungal, antioxidant, cytotoxic, antitumor and chemopreventive activities. Previously published reviews on this topic survey the biological activities of natural and synthetic chalcones but there are no comprehensive contributions on occurrence and biological activities of natural chalcones. The present study provides an overview of hydroxy or/and methoxy-substituted chalcones, methylated, prenylated, geranylated and other monomeric derivatives, chromeno- and furanochalcones, dimeric chalcones and dihydrochalcone derivatives focusing on their biosynthesis, natural sources and biological activities. On the basis of 608 references, this review covers the phytochemistry and biological activity of natural chalcones, describing 646 compounds have been appeared in the literature since 1975. The summary is aimed to initiate further pharmacobotanical, biotechnological and medicinal studies on the field of chalcone research. This contribution reviews some of the general aspects of naturally occurring chalcones including their chemical categories, focusing on plant sources and biological activities. The review covers the major works appeared in the literature from 1975 up to 2014, relating to 608 references and 646 compounds.

228 citations

Journal ArticleDOI
21 Jun 2016
TL;DR: An appraisal of flavone formation in plants is appraised, emphasizing the emerging theme that biosynthesis pathway determines flavone chemistry.
Abstract: Flavones correspond to a flavonoid subgroup that is widely distributed in the plants, and which can be synthesized by different pathways, depending on whether they contain C- or O-glycosylation and hydroxylated B-ring. Flavones are emerging as very important specialized metabolites involved in plant signaling and defense, as well as key ingredients of the human diet, with significant health benefits. Here, we appraise flavone formation in plants, emphasizing the emerging theme that biosynthesis pathway determines flavone chemistry. Additionally, we briefly review the biological activities of flavones, both from the perspective of the functions that they play in biotic and abiotic plant interactions, as well as their roles as nutraceutical components of the human and animal diet.

206 citations