Thermal Rearrangement of Azido Ketones into Oxazoles via Azirines: One-Pot, Metal-Free Heteroannulation to Functionalized 1,3-Oxazoles


Autoria(s): Shah, Shailesh R; Navathe, Sudhanva S; Dikundwar, Amol G; Row, Tayur Guru N; Vasella, Andrea T
Data(s)

2013

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