Simple exploration of 144750-42-5

Reference of 144750-42-5, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 144750-42-5.

Reference of 144750-42-5, Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, 144750-42-5, Name is (S)-2-(2-Chlorophenyl)-2-(6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetic acid hydrochloride, SMILES is O=C(O)[C@H](C1=CC=CC=C1Cl)N2CCC3=C(C=CS3)C2.[H]Cl, belongs to pyridine-derivatives compound. In a article, author is Gonzalez-Silva, Karen, introduce new discover of the category.

Copper(ii) accelerated azide-alkyne cycloaddition reaction using mercaptopyridine-based triazole ligands

We report the preparation and full characterization of a series of mercapto pyridine-functionalized 1,2,3-triazoles and their use as ligands for the preparation of copper(ii) complexes. Complex 1 supported by a 2-mercaptopyridine functionalized triazole (A) and featuring a polymeric structure with the coordination of CuCl2 centers at both the triazole and pyridine fragments, displays a highly effcient click-type catalytic performance in alcoholic solvents without the need for an external reducing agent. Experimental results suggest that the copper(ii) species undergo reduction to catalytic copper(i) via alcohol oxidation during an induction period. The scope of the click reaction is broad including the high yielding synthesis of a series of mono, bis, and tris-triazoles, using microwave radiation under low catalyst loadings.

Reference of 144750-42-5, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 144750-42-5.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem