Chemistry is an experimental science, Application In Synthesis of Piperidine-2,6-dione, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 1121-89-7, Name is Piperidine-2,6-dione
Reactions of beta-chlorovinylcarbonyl compounds 10, 14, 16, 18, 20, 22, with sodium dicarbonyl-eta5-cyclopentadienyl-ferrate (NaFp) furnish beta-acylvinyl-dicarbonyl-eta5-cyclopentadienyl-iron complexes 15, 17, 19, 21, 23 and binuclear iron complexes 26-29.Spectral data demonstrate the donor effect of the Fp group.Irradiation of these complexes in the presence of triphenylphosphane delivers beta-acylvinyl-carbonyl-eta5-cyclopentadienyl-triphenylphosphane-iron complexes 34, 35.Reaction of glutarimides with oxalyl chloride gives rise to oxazolo<3,2a>pyridines 13.Benzylidenemalonyl chloride reacts with FpCS2Na to form benzylidenethietane-2,4-dione (32).A beta-acylethinyl-carbonyl-eta5-dicyclopentadienyl-iron complex 43 has been prepared.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application In Synthesis of Piperidine-2,6-dione, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 1121-89-7, in my other articles.
Reference：
Piperidine – Wikipedia,
Piperidine | C5H1346N – PubChem