Thermal Rearrangement of Azido Ketones into Oxazoles via Azirines: One-Pot, Metal-Free Heteroannulation to Functionalized 1,3-Oxazoles
Data(s) |
2013
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Resumo |
alpha-Azidoacetophenones were converted into 2-aryl-1,3-oxazole-4-carbaldehydes through rearrangement of the carbon framework upon exposure to DMF/POCl3. The unprecedented rearrangement occurs via alkenyl azides and 2H-azirines. A mechanism for this unusual reaction was proposed and evidenced. |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/46408/1/eur_jl_org_che_2_264_2013.pdf Shah, Shailesh R and Navathe, Sudhanva S and Dikundwar, Amol G and Row, Tayur Guru N and Vasella, Andrea T (2013) Thermal Rearrangement of Azido Ketones into Oxazoles via Azirines: One-Pot, Metal-Free Heteroannulation to Functionalized 1,3-Oxazoles. In: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2). pp. 264-267. |
Publicador |
WILEY-V C H VERLAG GMBH |
Relação |
http://dx.doi.org/10.1002/ejoc.201201269 http://eprints.iisc.ernet.in/46408/ |
Palavras-Chave | #Solid State & Structural Chemistry Unit |
Tipo |
Journal Article PeerReviewed |