Brief introduction of 112068-01-6

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Application In Synthesis of (S)-Diphenyl(pyrrolidin-2-yl)methanol, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 112068-01-6

Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 112068-01-6, molcular formula is C17H19NO, introducing its new discovery. Application In Synthesis of (S)-Diphenyl(pyrrolidin-2-yl)methanol

We employed the membrane of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) liposomes suspended in water as a microenvironment for carrying out the organocatalytic epoxidation of an alpha-alkylidene oxindole. The reaction proceeds smoothly and displays diastereo- and enantio-selectivity that differs from what is achieved under bulk solution conditions. The potential of organocatalytic approaches for synthetic transformations in aqueous phase in the presence of dispersed membranes is briefly discussed.

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Application In Synthesis of (S)-Diphenyl(pyrrolidin-2-yl)methanol, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 112068-01-6

Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI