1996
DOI: 10.1039/p19960000147
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A one-step photocatalytic synthesis of 2-(trifluoromethyl)butyrolactones

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Cited by 12 publications
(3 citation statements)
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“…TiO 2 59-67 and also other catalysts [67][68][69][70][71][72] have been applied to many conversions, generally in organic solvent, although a few syntheses were performed in water 63 or ethanol. 64…”
Section: Other Reactionsmentioning
confidence: 99%
“…TiO 2 59-67 and also other catalysts [67][68][69][70][71][72] have been applied to many conversions, generally in organic solvent, although a few syntheses were performed in water 63 or ethanol. 64…”
Section: Other Reactionsmentioning
confidence: 99%
“…Treatment with Raney nickel produced the desired 2-trifluoromethylbutyrolactone 8. 12 Similarly, dimethyl malonate 1a afforded the known dimethyl 2-trifluoromethylmalonate 4a. 13 Strong steric hindrance to the carbon a to the carboxylate moiety as in butyl neopentanoate 1b is responsible for low yields of the corresponding 1,1-bis(methyl sulfide) 2b (20%), but the reactions with BrF 3 and Raney nickel proceed as expected resulting in butyl 2-trifluoromethyl-a-t-butyl acetate 4b.…”
mentioning
confidence: 98%
“…This ring system, known also as furanone or butenolide [1], occurs as structural subunits in a large number of natural products isolated from many sources including sponges and algas [2], animals [3], plants [4], butterflies [5] and others insects [6]. This ring system has also been the target of many synthesis due its potential pharmaceutical and industry proprieties [18], as intermediate in synthesis of antibodies, as selective catalysts [19], as dopants for ferroelectric liquid crystals [20] and as monomers for ring-opening polymerization to generate polyesters as potential piezo-electric material [21]. This ring system has also been the target of many synthesis due its potential pharmaceutical and industry proprieties [18], as intermediate in synthesis of antibodies, as selective catalysts [19], as dopants for ferroelectric liquid crystals [20] and as monomers for ring-opening polymerization to generate polyesters as potential piezo-electric material [21].…”
Section: Introductionmentioning
confidence: 99%