4435-33-0Relevant articles and documents
A TEMPO-like nitroxide combined with an alkyl-substituted pyridine: An efficient catalytic system for the selective oxidation of alcohols with iodine
Kashparova, Vera P.,Klushin, Victor A.,Zhukova, Irina Yu.,Kashparov, Igor S.,Chernysheva, Daria V.,Il'chibaeva, Irina B.,Smirnova, Nina V.,Kagan, Efim Sh.,Chernyshev, Victor M.
supporting information, p. 3517 - 3521 (2017/10/05)
An efficient method for the oxidation of alcohols to aldehydes or ketones in a two-phase CH2Cl2/NaHCO3 (aq.) system, using iodine and catalytic amounts of 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxyl and 2,4,6-trimethylpyridine, was developed. The performance of the method was demonstrated by the selective oxidation of 37 variously substituted alcohols in ≥90% yield, including the gram-scale synthesis of the important chemical 2,5-diformylfuran from biomass-derived 5-hydroxylmethylfurfural.
STUDY OF THE HYDROLYTIC STABILITY OF 1-ANILINO-1-ALKANESULFONATES BY MEANS OF SPECTRODENSITOMETRIC THIN-LAYER CHROMATOGRAPHY
Nesterenko, S. A.,Bogatchuk, Yu. Ya.,Kofanov, V. I.
, p. 1666 - 1670 (2007/10/02)
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