Journal
NEW JOURNAL OF CHEMISTRY
Volume 38, Issue 12, Pages 5727-5735Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4nj01101e
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Funding
- Department of Science and Technology (DST), New Delhi [SR-S1/OC-60/2011]
- Board of Research in Nuclear Sciences (BENS)
- Department of Atomic Energy (DAB)
- Government of India [2012/37C/3/BRNS]
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Annulation of enamides into 2,5- and 2,4,5-substituted oxazoles by NBS/Me2S in the presence of mild base has been achieved. The reaction conditions are simple and tolerant to a wide variety of substituents including both electron-donating and withdrawing groups to produce oxazotes in one-pot without further purification of the intermediate.
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