Abstract
A new series of 5,6-dihydro-4H-1,2-oxazines were synthesized via hetero Diels-Alder reaction of α-nitrosoolefins with alkenes. α-Nitrosoolefins were generated from ketoximes by the action of chloramine-T. The newly synthesized compounds were characterized with IR, NMR, elemental analysis and screened for their antimicrobial activity; they exhibited excellent antimicrobial activity. The minimal inhibitory concentration of the compounds was in the range of 10-35 μg ml-1 for bacteria and 10-40 μg ml-1 for fungi.
Original language | English |
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Pages (from-to) | 280-288 |
Number of pages | 9 |
Journal | European Journal of Medicinal Chemistry |
Volume | 44 |
Issue number | 1 |
DOIs | |
Publication status | Published - 01-2009 |
All Science Journal Classification (ASJC) codes
- Pharmacology
- Drug Discovery
- Organic Chemistry