25315-30-4Relevant academic research and scientific papers
I 2 /TBHP-Promoted Approach to α-Keto Esters from Trifluoromethyl β-Diketones and Alcohols via C-C Bond Cleavage
Shao, Tongle,Fang, Xiang,Zhou, Jun,Jin, Chen,Yang, Xueyan,Wu, Fanhong
, p. 2018 - 2023 (2017)
A metal-free oxidative coupling reaction of trifluoromethyl β-diketones with alcohols for the synthesis of α-keto esters in good to excellent yields has been developed. Preliminary mechanistic studies suggest that an I 2 /TBHP promoted sequential iodination, C-C bond cleavage, C-O bond formation and oxidation pathway is involved in this reaction.
MICROCAPSULES CONTAINING A GAS-GENERATING PHOTOLABILE POLYMER AND USES THEREOF
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Paragraph 0172-0174, (2017/09/30)
The present invention relates to water-dispersable microcapsules comprising an oil phase, e.g. a perfume, containing a photolabile polymer comprising α-ketoacid or α-ketoester group capable of generating a gas upon exposure to light. The gas is able to ca
Cu-catalyzed esterification reaction via aerobic oxygenation and C-C bond cleavage: An approach to α-ketoesters
Zhang, Chun,Feng, Peng,Jiao, Ning
supporting information, p. 15257 - 15262 (2013/11/06)
The Cu-catalyzed novel aerobic oxidative esterification reaction of 1,3-diones for the synthesis of α-ketoesters has been developed. This method combines C-C σ-bond cleavage, dioxygen activation and oxidative C-H bond functionalization, as well as provides a practical, neutral, and mild synthetic approach to α-ketoesters which are important units in many biologically active compounds and useful precursors in a variety of functional group transformations. A plausible radical process is proposed on the basis of mechanistic studies.
Photochemical Reactions of Halo-/Aryl Sulfide-Substituted Alkyl Phenylglyoxylate, an Assessment of the Lifetime of the Intermediate 1,4-Biradical
Hu, Shengkui,Neckers, Douglas C.
, p. 7827 - 7831 (2007/10/03)
Photochemical reactions of several halo/aryl sulfide-substituted alkyl phenylglyoxylates (1) were studied. For 2′-bromo- (1b), 2′-iodo- (1c), 2′-(phenylthio)- (1d), and 2′-(phenylsulfinyl)- (1e) ethyl phenylglyoxylate, vinyl phenylglyoxylate (2), proposed to be the result of β-elimination from the 1,4-biradical formed by triplet state γ-hydrogen abstraction, is the dominant photoproduct. In the cases 1b and Id Norrish Type II products were also observed. Vinyl phenylglyoxylate (2) was not observed with 2′-chloroethyl (1a), 3′-bromopropyl (1f), and 3′-(phenylthio)propyl (1g) phenylglyoxylate. The lifetime of the 1,4-biradical intermediate is deduced from the competition between the β-elimination of the monoradical and the normal biradical decay. The triplet lifetime and the photoreaction efficiency of 1 were not significantly affected by halogen-substitution.
