In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Intramolecular, Intermolecular, and Heterogeneous Nonadiabatic Dissociative Electron Transfer to Peresters, published in 2001-10-03, which mentions a compound: 3685-23-2, Name is cis-4-Aminocyclohexane carboxylic acid, Molecular C7H13NO2, Safety of cis-4-Aminocyclohexane carboxylic acid.
The electron transfer to peresters was studied by electrochem. means in N,N-dimethylformamide. The reduction was carried out by three independent methods: (i) heterogeneously, by using glassy carbon electrodes, (ii) homogeneously, by using electrogenerated radical anions as the donors, and (iii) intramolecularly, by using purposely synthesized donor-spacer-acceptor (D-Sp-A) systems (tert-Bu 1,3-dihydro-α,α-di-Methyl-1,3-dioxo-peroxy-2H-isoindole-2-acetate and tert-Bu cis-4-Phthalimidocyclohexanepercarboxylate). Convolution anal. of the heterogeneous data led to results in excellent agreement with the dissociative electron transfer theory. The homogeneous redox catalysis data also confirmed the reduction mechanism. The cyclic voltammetries of the D-Sp-A mols. could be simulated, leading to determination of the corresponding intramol. dissociative rate constants Anal. of the results showed that, regardless of the way by which the acceptor is reduced, the investigated dissociative electron transfers are strongly nonadiabatic and, particularly, that the exptl. rates are several orders of magnitude smaller than the adiabatic limit. A possible mechanism responsible for the observed behavior is discussed.
The article 《Intramolecular, Intermolecular, and Heterogeneous Nonadiabatic Dissociative Electron Transfer to Peresters》 also mentions many details about this compound(3685-23-2)Safety of cis-4-Aminocyclohexane carboxylic acid, you can pay attention to it, because details determine success or failure
Reference:
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate