50768-10-0Relevant academic research and scientific papers
Synthesis of functionalised cyclopentenones via rearrangement of pyranones
Caddick, Stephen,Cheung, Steven,Frost, Lisa M.,Khan, Safraz,Pairaudeau, Garry
, p. 6879 - 6882 (2000)
Substituted functionalised cyclopentenones could be obtained via base-mediated isomerisation of pyranones. (C) 2000 Elsevier Science Ltd.
Process for the production of tetrahydropyran-3-one derivatives
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, (2008/06/13)
A process for producing a tetrahydropyran-3-one derivative of the formula: STR1 wherein R is a hydrogen atom; a straight chained or branched C1 -C10 alkyl group which is unsubstituted or substituted by a halogen atom, a hydroxyl group, a C1 -C6 alkoxy group, a C1 -C6 alkylthio group, a C1 -C6 alkylcarbonyloxy group, a C1 -C6 alkoxycarbonyl group, a C1 -C6 mono- or dialkylamino group, a C3 -C6 cycloaklyl group, a C1 -C6 alkylaminocarbonyl group, a C1 -C6 alkylcarbonylamino group, a C1 -C6 alkylcarbonyl group or a phenyl or benzoyl group which is unsubstituted or substituted by a halogen atom, a C1 -C6 alkyl group, a C1 -C6 alkoxy group, a C1 -C6 alkythio group or a C1 -C6 alkoxycarbonyl group; a C3 -C6 cycloalkyl group; or a phenyl or biphenyl group which is unsubstituted or substituted by a halogen atom, a C1 -C6 alkoxy group or C1 -C6 alkylthio group, which comprises reacting a 2H-pyran-3(6H)-one derivative of the formula: STR2 wherein R is as defined above, and R' is a straight chained or branched C1 -C6 acyl group which is unsubstituted or substituted by a halogen atom; a benzoyl group; a C1 -C6 alkoxycarbonyl group; or a mono- or dialkylaminocarbonyl group which is unsubstituted or substituted by a C1 -C3 alkyl group or a phenyl group, with hydrogen in the presence of a catalyst selected from the group consisting of cobalt, nickel, ruthenium, rhodium, palladium, iridium, platinum and copper chromite.
Oxidation of furans. 2. Synthesis and biological properties of 6 hydroxy 2H pyran 3(6H) ones and derivatives
Laliberte,Medawar,Lefebvre
, p. 1084 - 1089 (2007/10/08)
The anticoccidial and in vitro antimicrobial properties of a series of 6 hydroxy 2H pyran 3(6H) ones VI and theirderivatives were investigated. Compounds VI were readily prepared by the peracid oxidation of the appropriate 2 furanmethanols. Activity was m
