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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.


Papers
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Journal ArticleDOI
TL;DR: Synthesis and physico-chemical properties of two 3-substituted phenacyl-thiazolidine-2,4-diones (2c-d) and four 3- substituting phenacy l-5-[2-phenyl-4H-4-oxo-1-benzopyran-6-yl)methyl-enyl]- thiazolidin e- 2, 4- diones are described.
Abstract: Synthesis and physico-chemical properties of two 3-substituted phenacyl-thiazolidine-2,4-di-ones (2c-d) and four 3-substituted phenacyl-5-[2-phenyl-4H-4-oxo-1-benzopyran-6-yl)methyl-enyl]-thiazolidine-2.4-diones (4a-d) are described. These products were synthesized by Knoevenagel reaction from flavone-6-carboxaldehydc (3) and 3-(substituted phenacyl)-thiazolidine-2,4-diones (2a-d). Antibacterial and antifungal activities were investigated for these compounds.

7 citations

Patent
Katoh Susumu1, Shinsuke Sayama1, Saizo Shibata1, Itsuo Uchida1, Yamaki Tokuo1 
24 Apr 1992
TL;DR: A benzopyran derivative represented by general formula (I) and a pharmaceutically acceptable salt thereof, wherein each symbol is as defined in the specification, is useful for treating hypertension, because it has a persistent hypotensive activity and a peripheral blood relaxing activity by activating a potassium channel, and also for treating cardiovascular diseases such as angina pectoris and heart failure as discussed by the authors.
Abstract: A novel benzopyran derivative represented by general formula (I) and a pharmaceutically acceptable salt thereof, wherein each symbol is as defined in the specification. This compound is useful for treating hypertension, because it has a persistent hypotensive activity and a peripheral blood relaxing activity by activating a potassium channel, and also for treating cardiovascular diseases such as angina pectoris and heart failure, because it has a selective coronary blood stream increasing activity.

7 citations

Journal ArticleDOI
TL;DR: In this paper, the stereochemical correlations including the configurations of the ring juncture and the methyl group and also the ring conformations of these six lactones were investigated by chemical means and by nuclear magnetic resonance (NMR) spectrometry, such as two-dimensional(2D) NMR and steady-state 1H-1H nuclear Overhauser effect experiments.
Abstract: Four stereoisomers of 3-methyloctahydroisocoumarins (4a-d)and two 1-methyloctahydro-3H-2-benzopyran-3-ones (10a, b) were synthesized. The stereochemical correlations including the configurations of the ring juncture and the methyl group and also the ring conformations of these six lactones were investigated by chemical means and by nuclear magnetic resonance (NMR) spectrometry, such as two-dimensional(2D) NMR and steady-state 1H-1H nuclear Overhauser effect experiments. It was concluded that the lactone ring of 4b, c, and 10a adopts a boat or a slightly distorted boat conformation in solution.

7 citations

Journal ArticleDOI
TL;DR: The photochromism of [7-hydroxy-8-formyl-3-methyl-4-oxospiro[1,3-benzoxazin-2,2 ǫ]-[2H-1]benzopyran],SP(I),SP(II) and their coordination with Tb3.
Abstract: The photochromism of [7-hydroxy-8-formyl-3-methyl-4-oxospiro[1,3-benzoxazin-2,2-[2H-1]benzopyran],SP(I),[7-hydroxy-8-formyl-3-benzyl-4-oxospiro[1,3-benzoxazin-2,2-[2H-1]benzopyran] SP(II) and their coordination with Tb3

7 citations


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