135206-85-8Relevant articles and documents
Simple chemoenzymatic access to enantiopure pharmacologically interesting (R)-2-hydroxypropiophenones
Demir, Ayhan S.,Hamamci, Haluk,Sesenoglu, Ozge,Aydogan, Feray,Capanoglu, Doga,Neslihanoglu, Rahsan
, p. 1953 - 1956 (2007/10/03)
A chemoenzymatic synthesis of pharmacological interesting (R)-2-hydroxypropiophenones starting from propiophenone derivatives is described. Manganese(III) acetate-mediated acetoxylation followed by fungus-mediated hydrolysis of propiophenone derivatives affords (R)-2-hydroxypropiophenones in high enantiomeric excess.
Decomposition of α-hydroxyaryl ketones and characterization of some unusual products
Gala,Puar,Das,Kugelman,DiBenedetto
, p. 1199 - 1203 (2007/10/02)
α-Hydroxyaryl ketones such as 2-hydroxypropiophenone and 1-(2,4- difluorophenyl)-2-hydroxy-1-propanone, the key intermediates in the preparation of antifungal agents, decompose into oxidized, rearranged, and condensed products. These products were isolated and characterized. The possible mechanisms for the formation of the products are discussed.