Huang, Gaochao; Shrestha, Ruben; Jia, Kaimin; Geisbrecht, Brian V.; Li, Ping published the artcile< Enantioselective Synthesis of Dilignol Model Compounds and Their Stereodiscrimination Study with a Dye-Decolorizing Peroxidase>, Synthetic Route of 171877-39-7, the main research area is dilignol model compound enantioselective preparation surface plasmon resonance TcDyP.
A four-step enantioselective approach was developed to synthesize anti (1R,2S)-I and (1S,2R)-I containing a β-O-4 linkage in good yields. A significant difference was observed for the apparent binding affinities of four stereospecific lignin model compounds with TcDyP by surface plasmon resonance, which was not translated into a significant difference in enzyme activities. The discrepancy may be attributed to the conformational change involving a loop widely present in DyPs upon H2O2 binding.
Organic Letters published new progress about Diastereoselective synthesis. 171877-39-7 belongs to class thiazole, and the molecular formula is C10H11NS2, Synthetic Route of 171877-39-7.
Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica