Extracurricular laboratory: Synthetic route of 132098-59-0

Although many compounds look similar to this compound(132098-59-0)Quality Control of Bis((S)-4-phenyl-4,5-dihydrooxazol-2-yl)methane, numerous studies have shown that this compound(SMILES:C1(CC2=N[C@@H](C3=CC=CC=C3)CO2)=N[C@@H](C4=CC=CC=C4)CO1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: Bis((S)-4-phenyl-4,5-dihydrooxazol-2-yl)methane, is researched, Molecular C19H18N2O2, CAS is 132098-59-0, about Improvement of ligand economy controlled by polymer morphology: The case of polymer-Supported bis(oxazoline) catalysts, the main research direction is enantioselective polymer supported bisoxazoline catalyst preparation morphol; organic reaction enantioselective polymer Supported bisoxazoline catalyst.Quality Control of Bis((S)-4-phenyl-4,5-dihydrooxazol-2-yl)methane.

A functionalized chiral bis(oxazoline) is used as a chiral monomer in polymerization reactions leading to homo- and copolymers of different morphol. Polymers with a high content of chiral monomer lead to enantioselectivities that are higher than those obtained with the soluble ligand, but the chiral ligand is not used in an optimal way. A hyperbranched polymer, obtained by using a hexavinyl dendrimer as the cross-linker, leads to the same enantioselectivities with a more efficient use of the chiral ligand.

Although many compounds look similar to this compound(132098-59-0)Quality Control of Bis((S)-4-phenyl-4,5-dihydrooxazol-2-yl)methane, numerous studies have shown that this compound(SMILES:C1(CC2=N[C@@H](C3=CC=CC=C3)CO2)=N[C@@H](C4=CC=CC=C4)CO1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles