A new synthetic route of 560-09-8

If you want to learn more about this compound((1S,3R)-1,2,2-Trimethylcyclopentane-1,3-dicarboxylic acid)Formula: C10H16O4, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(560-09-8).

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 560-09-8, is researched, Molecular C10H16O4, about A Tale of Three Carboxylates: Cooperative Asymmetric Crystallization of a Three-Dimensional Microporous Framework from Achiral Precursors, the main research direction is manganese formate adamantanedicarboxylate polymer preparation chirality camphoric glutamic; crystal structure manganese formate adamantanedicarboxylate chirality induction; gas adsorption manganese formate adamantanedicarboxylate polymer complex.Formula: C10H16O4.

Sym. crystallization of 3D porous materials constructed entirely from achiral building blocks by using enantiopure organic acids or amino acids as chirality-inducing agents is reported. Thus, the presence of D-camphor led to (+)-Mn3(HCOO)4(adc) (adc = 1,3-adamantanedicarboxylate), while L-camphor resulted in (-)-Mn3(HCOO)4(adc), which were characterized by x-ray crystallog. The chiral induction agent is essential to initiate the nucleation of the chiral crystals. The chirality control seems to be achieved through cooperative binding between enantiopure chiral reagents and achiral structural building units. Enantiopure chiral reagents control the absolute chirality of the crystals by participating in the nucleation and crystallization processes, but are later replaced with achiral ligands in the resulting crystals.

If you want to learn more about this compound((1S,3R)-1,2,2-Trimethylcyclopentane-1,3-dicarboxylic acid)Formula: C10H16O4, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(560-09-8).

Reference:
Isothiazole – Wikipedia,
Isothiazole – ScienceDirect.com