155878-90-3Relevant articles and documents
Preparation of new 2,4-disubstituted oxazoles from N-acylaziridines
Eastwood, Frank W.,Perlmutter, Patrick,Yang, Qi
, p. 35 - 42 (2007/10/03)
The efficiency of the ring enlargement of 2-substituted N-acylaziridines to dihydrooxazoles followed by nickel peroxide oxidation to give 2,4-disubstituted oxazoles as a synthetic route is examined. Sodium iodide-promoted ring enlargements work well for N-acylaziridines bearing electron-donating 2-substituents. For N-acylaziridines bearing electron-withdrawing 2-substituents, the best results are obtained using acid-promoted rearrangement.
Preparation of new 2,4-disubstituted oxazoles
Eastwood,Perlmutter,Yang
, p. 2039 - 2042 (2007/10/02)
Ring enlargement of N-acylaziridines followed by nickel peroxide oxidation provides a variety of 2,4-disubstituted-1,3-oxazoles suitable for bis- and tris-oxazole synthesis.