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Synthesis and antimicrobial activity of some methyl-2-[N-coumarin-6′-yl]-3-oxo-2,3-dihydro-1H-isoindolone-5-carboxylates

✍ Scribed by Aabid Ali Mir; Vinata V. Mulwad; G. K. Trivedi


Book ID
102342985
Publisher
Journal of Heterocyclic Chemistry
Year
2009
Tongue
English
Weight
164 KB
Volume
47
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

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N‐substituted furylmethylimines are prepared by condensing 6‐aminocoumarins with furfural, these on sodium borohydride reduction afford N‐[coumarin‐6′‐yl]‐2‐furylamines. Intramolecular [4+2] cycloaddition of these amines with maleic anhydride results into 3‐[N‐coumarin‐6′‐yl]‐4‐oxo‐10‐oxa‐3‐azatricyclo[5.2.1.0^1.5^]dec‐8‐ene‐6‐carboxylic acids 4a, 4b, 4c. The [4+2] cycloadducts on p‐toluene sulphonic acid treatment followed by esterification yield the titled compounds. Compound 5a, 5b, 5c was also reduced to isoindolone alcohol 7a, 7b, 7c by sodium borohydride in the presence of a base. All the compounds have been tested in vitro for their antimicrobial activity against gram‐positive bacteria Bacillus subtilis, Staphylococcus aureus, one gram‐negative bacteria, Escherichia coli, and one fungal strain Candida albicans at 100 μg/mL concentration. J. Heterocyclic Chem., 2010.


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ChemInform Abstract: Synthesis and Antim
✍ Aabid Ali Mir; Vinata V. Mulwad; G. K. Trivedi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 40 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

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✍ Vinata V. Mulwad; Sagar A. Mayekar 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 36 KB 👁 1 views

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