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Oxazolines were introduced by Meyers as intermediates for synthesis of ß-hydroxy acids or esters, by alkylation of the lithio-derivative and cleavage of the ring. Similarly, addition to carbonyl compounds leads, under dehydrating conditions (strong acid) to the corresponding acrylic acids: J. Org. Chem., 39, 2778 (1974):/n
Reaction with epoxides leads to -butyrolactones: J. Org. Chem., 39, 2783 (1974)./n
Substituted ß-keto esters can be prepared by reaction with an acid chloride followed by the introduction of further substituents by alkylation of the acylated oxazoline in DMF: Bull. Chem. Soc. Jpn., 57, 2329 (1984):/n
For reviews of the chemistry of oxazolines, see: Chem. Rev., 71, 483 (1971); Angew. Chem. Int. Ed., 15, 270 (1976), Tetrahedron, 41, 837 (1985); 50, 2297 (1994)./n
Dichiarazioni di rischio (UE): H225
Highly flammable liquid and vapour.
Dichiarazioni precauzionali: P260-P201-P280a-P304+P340-P405-P501a
Do not breathe dust/fume/gas/mist/vapours/spray. Obtain special instructions before use. Wear protective gloves and eye/face protection. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.