Jouanno, Laurie-Anne published the artcileExpeditious Microwave-Assisted Synthesis of 5-Alkoxyoxazoles from α-Triflyloxy Esters and Nitriles, Safety of Ethyl 2-Iodopropionate, the publication is Journal of Organic Chemistry (2012), 77(19), 8549-8555, database is CAplus and MEDLINE.
A rapid and general access to diversely substituted 5-alkoxyoxazoles from easily accessible α-triflyloxy/hydroxy esters and nitriles with good yields (41-76%) is reported. The versatility of the cyclization is shown for a range of substrates with high selectivity toward triflates over tosylates and proved to be compatible with sensitive functional groups. As an illustration of this transformation, the first synthesis of the recently isolated hydroxypyridine Me multijuguinate (I) was achieved in four steps through a hetero Diels-Alder reaction of the 5-alkoxyoxazole II and acrylic acid, followed by a protodecarboxylation reaction.
Journal of Organic Chemistry published new progress about 31253-08-4. 31253-08-4 belongs to iodides-buliding-blocks, auxiliary class Iodide,Ester, name is Ethyl 2-Iodopropionate, and the molecular formula is C5H9IO2, Safety of Ethyl 2-Iodopropionate.
Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com