Chemistry and application of 4-oxo-4H-1-benzopyran-3- carboxaldehyde
TLDR
The publications on the title compound appearing mainly since 2007 to February 2014 are reviewed in this article, where the authors present a review of the most relevant publications on this title compound, mainly from 2007 to 2014.Abstract:
The publications on the title compound appearing mainly since 2007 to February 2014 are reviewed.read more
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Synthesis, characterization, DNA-binding studies and acetylcholinesterase inhibition activity of new 3-formyl chromone derivatives
TL;DR: A series of new substituted 3-formyl chromone derivatives (4-6) were synthesized by one step reaction methodology by knoevenagel condensation, structurally similar to known bisintercalators and it was found that synthesized compounds, especially compound 6 (evident from binding constant value) bind strongly with calf thymus DNA, presumably via an intercalation mode.
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Synthesis of polyfunctionalized benzophenones via the reaction of 3-formylchromones with tertiary push–pull enamines
TL;DR: In this article, a nucleophilic reaction of 3-formylchromones with tertiary push-pull enamines in refluxing acetonitrile gave polyfunctionalized benzophenone derivatives as a result of a [3+3] annulation in moderate to good yields.
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Synthesis and chemical properties of thiochromone and its 3-substituted derivatives (review)
TL;DR: In this paper, a review article contains generalized and systematically arranged data about the methods of synthesis and the reactivity of thiochromone and its 3-substituted derivatives over the previous 40 years.
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Synthesis of heterocyclic analogs of isoflavone and homoisoflavone based on 3-formylchromone.
Stanislav S. Shatokhin,Vladislav A. Tuskaev,Vladislav A. Tuskaev,S. Ch. Gagieva,Eduard T. Oganesyan +4 more
TL;DR: In this article, a review of recent developments of chemistry of synthetic analogs of natural compounds, isoflavone and homoisoflavones, is presented, with a focus on the application of modern strategies of organic synthesis, namely green chemistry approaches, click reactions, domino reactions, etc.
References
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Synthesis, structural characterization, fluorescence, antimicrobial, antioxidant and DNA cleavage studies of Cu(II) complexes of formyl chromone Schiff bases.
TL;DR: Antimicrobial, antioxidant and DNA cleavage activities indicate that metal complexes exhibited greater activity as compared with ligands, and distorted octahedral geometry is proposed for all the Cu(II) complexes.