485755-70-2Relevant academic research and scientific papers
Reactivity of alicyclic 1,5,9-triketones toward five-, six-, and seven-membered rings in acidic medium. Stereochemistry of intramolecular cyclization products
Akimova, Taisia I.,Soldatkina, Olga A.,Gerasimenko, Andrey V.,Savchenko, Vyacheslav G.,Kapustina, Alevtina A.
, p. 1079 - 1085 (2022/01/11)
[Figure not available: see fulltext.] Among nine alicyclic 1,5,9-triketones with differently fused 5-, 6-, and 7-membered rings in the molecule, existing as mixtures of 3–6 diastereomers, only those containing at least two 6-membered rings were capable of
Methods of synthesis of alicyclic 1,5,9-triketones. Reaction of transaminomethylation
Akimova,Soldatkina,Ivanenko, Zh. A.,Savchenko
, p. 720 - 728 (2017/07/07)
Alicyclic 1,5,9-triketones with various combination of 5-, 6-, 7-membereded cycles in the molecule were obtained by methods of diketone condensation, Michael reaction, and proceeding from Mannich mono- and bisbases and cycloalkanones. The latter method wa
An alicyclic 1,5,9-triketone 2,6-bis[(2-oxocyclohexyl)methyl]cyclohexanone, its cyclic form and reactions with N-nucleophiles
Akimova, Taisia I.,Kravchenko, Natalia S.,Denisenko, Vladimir A.
, p. 9548 - 9554 (2008/12/22)
The alicyclic 1,5,9-triketone 2,6-bis[(2-oxocyclohexyl)methyl]cyclohexanone, its cyclic form, and the product of its dehydration have been studied under Leuckart reaction conditions, with ammonium acetate in acetic acid and with hydroxylamine. The composi
