## Abstract A facile oneβpot synthesis of oxazoles 1aβh is described that utilizes readily available aromatic Ξ±βmethyl ketones and a safe hypervalent iodine reagent, iodobenzene diacetate.
A general, one-pot method for the synthesis of 2-substituted oxazoles
β Scribed by Eric L. Williams
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- French
- Weight
- 238 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The reaction of 2-irimcihylsilyi-1,2,3-triazole with acid chlorides readily forms iriazuie amides. The wiazole amides, when heated 10 15oOC in suifolane. rearrange wirh rhe elimination of niwngen to give 2-subslituied nxazoles in high yields. The nxazoie synlhesis is general. and can be carried 01~1 in one-pot.
π SIMILAR VOLUMES
## A general , totally stereoselectrve one-pot synthesis of cls-3-substttuted-+formylazetrdtn-2-ones based upon the reacuon of actd chlorides and 1,4-b~s-(4-methoxyphenyl)-I,4-drazabuta-IJ-d~ene, as synthettc equrvalent of the correspondmg unknown a-formyhmtne, has been developed Appropnately as-s