134645-34-4Relevant academic research and scientific papers
Spectrophotometric study of kinetics of oxidation of oximes of 3,5-dimethyl-2,6-diarylpiperidin-4-ones with quinolinium fluorochromate
Vimala,Jani Bai
experimental part, p. 5699 - 5704 (2012/07/28)
The rate of oxidation of 3,5-dimethyl-2,6-diarylpiperidin-4-one oximes with quinolinium fluorochromate (QFC) was followed in aqueous acetic acid medium. The influence of substrate, oxidant, H+ ions, ionic strength and dielectric constant on the reaction rates at varied temperature has been studied. The stoichiometry is 1:1 and the product of oxidation is the corresponding ketone. Activation parameters have been computed and a suitable mechanism has been suggested.
A facile synthesis, antibacterial, and antitubercular studies of some piperidin-4-one and tetrahydropyridine derivatives
Aridoss, Gopalakrishnan,Amirthaganesan, Shanmugasundaram,Ashok Kumar, Nanjundan,Kim, Jong Tae,Lim, Kwon Taek,Kabilan, Senthamaraikannan,Jeong, Yeon Tae
scheme or table, p. 6542 - 6548 (2009/09/30)
The raise in clinical significance of multidrug-resistant bacterial pathogens has directed us to synthesize 2,6-diarylpiperidin-4-one and Δ3-tetrahydropyridin-4-ol based benzimidazole and O-arylsulfonyl derivatives. X-ray crystal structure of t
Conformational Analysis and 13C NMR Spectra of Some 2,6-Diarylpiperidin-4-ones
Hasan, Misbah Ul,Arab, Mohammad,Rajan, K. Pandia,Sekar, R.,Marko, Dale
, p. 292 - 295 (2007/10/02)
The 13C NMR spectra of several methyl substituted 2,6-diaryl-4-piperidones (aryl=phenyl, o-chlorophenyl) have been measured.Substituent parameters for methyl and chloro groups have also been derived and are discussed in terms of their steric and electroni
