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Chandrakanta Bandyopadhyay

Researcher at Centenary College of Louisiana

Publications -  90
Citations -  576

Chandrakanta Bandyopadhyay is an academic researcher from Centenary College of Louisiana. The author has contributed to research in topics: Benzopyran & Chromone. The author has an hindex of 13, co-authored 90 publications receiving 510 citations. Previous affiliations of Chandrakanta Bandyopadhyay include Bose Institute & Ramakrishna Mission Vivekananda Centenary College.

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Synthesis of Coumarin Derivatives from 4-Oxo-4H-1-benzopyran-3-carboxaldehyde via 3-(Arylaminomethylene)chroman-2,4-dione

TL;DR: K-10 Montmorillonite mediated condensation of aldehyde 1 with arylamine 2 affords chroman-2,4-dione 5 which gives tricoumarol 8 by acid hydrolysis, 4-arylamino-3-formylcoumarin 11 and 1-benzopyrano[4,3-b]quinoline 12 on heating with POCl3 as discussed by the authors.
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Rearrangements of N-alkyl-/aryl-nitrones derived from 4-oxo-4H-1-benzopyran-3-carboxaldehyde––a solvent-dependent process

TL;DR: In this paper, the synthesis of 1-benzopyrano[3,4d]isoxazole-4-one has been studied using 3-(alkyl-/aryl-aminomethylene)chroman-2,4-dione depending upon the reaction medium.
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Human response to blast-induced vibration and air-overpressure: an Indian scenario

TL;DR: In this article, a study of the human response to blasting in four mining localities across India has shown that the response is not simply political, as frequently assumed, irrespective of those questioned, a basic concern for the safety of property was the main response.
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Substituent-controlled domino-Knoevenagel-hetero Diels—Alder reaction— a one-pot synthesis of polycyclic heterocycles

TL;DR: The reaction of 2-(N-alkenyl-N-aryl)amino-4-oxo-4H-1-benzopyran-3-carbaldehyde with dimedone/Meldrum's acid/4-hydroxycoumarin by heating in ethanol in the presence of pyridine produces polycyclic heterocycles bearing pyrine and pyran rings in a one-pot reaction as discussed by the authors.
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Synthesis of bischromones by deformylative Mannich type reaction on chromone-3-carbaldehyde using α-aminoacid as the source of amine

TL;DR: In this paper, a deformylative Mannich type reaction was used to produce N-(chromone-3-ylmethyl)-N-methyl glycine or N,N-di(chromone 3-methyl)glycine.