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Benzopyran

About: Benzopyran is a research topic. Over the lifetime, 1889 publications have been published within this topic receiving 15235 citations.


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Journal ArticleDOI
TL;DR: A small library of glyco-fused benzopyran compounds has been synthesised and their interaction features with Aβ peptides have been characterised by using STD-NMR and trNOESY experiments.

39 citations

Journal ArticleDOI
TL;DR: The title aldehyde 1 in the presence of ammonia gives the pyridine derivatives 9-11 respectively with acetylacetone, diethyl malonate and ethyl cyanoacetate, and the coumarinopyridines 25 and 26, respectively as discussed by the authors.

39 citations

Journal ArticleDOI
TL;DR: An efficient and convenient procedure for the synthesis of benzopyran derivatives by one-pot condensation of substituted salicyaldehydes and substituted 1,3-hexanediones in the presence of a catalytic amount of 2,4,6-trichloro-1,3,5-triazine (TCT, cyanuric chloride) under solvent-free conditions was developed in this paper.

39 citations

Journal ArticleDOI
TL;DR: The conclusion of this experiment is that the synthesized compounds have varied and different influence on different classes of bacteria and the fungus C. albicans.
Abstract: Several novel 4-hydroxy-chromene-2-one derivatives 2b-16b were easily prepared through condensation reactions with microwave heating and characterized by elemental analysis, IR, 1H-NMR and mass spectrometry. Geometry optimization of these compounds was executed by PM3, PM5 and Minimize Energy methods to describe them via molecular descriptors. The antimicrobial activity of the synthesized compounds was evaluated against different microbial strains using two different methods: the diffusion method and the micro-dilution method. All data indicated that the products possess antimicrobial activity which depends on the nature of substituent attached to the benzopyran moiety. In general, after 24 h the MIC values of most tested coumarins was 0.13 mg/mL, but compounds 1 and 6b displayed the strongest antimicrobial activity on the tested cultures of bacteria after 48 h. Compound 13b has the strongest growth inhibitory potential on fungus C. albicans, tested by diffusion method,with an inhibition zone of 30-37 mm at a concentration of 150 µg/mL. The conclusion of this experiment is that the synthesized compounds have varied and different influence on different classes of bacteria and the fungus C. albicans.

38 citations

Journal ArticleDOI
TL;DR: The structure of clusifoliol isolated from whole plants of Peperomia clusiifolia has been established as 3,4-dihydro-2,7-dimethyl-6-(3-methyl-2-butenyl)-2-(4methyl-1,3-pentadienyl)2H-1-benzopyran-5-ol by spectroscopic methods.

38 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20234
202220
202114
20209
201925
201814