New discoveries in chemical research and development in 2021.In classical electrochemical theory, both the electron transfer rate and the adsorption of reactants at the electrode control the electrochemical reaction. In an article, author is Dorward, Kathryn M., once mentioned the application of 17924-92-4, Name is (S,E)-14,16-Dihydroxy-3-methyl-3,4,5,6,9,10-hexahydro-1H-benzo[c][1]oxacyclotetradecine-1,7(8H)-dione, molecular formula is C18H22O5, molecular weight is 318.3643, MDL number is MFCD00133085, category is pyrrolines. Now introduce a scientific discovery about this category, HPLC of Formula: https://www.ambeed.com/products/17924-92-4.html.
Suzuki-miyaura cross-coupling approach to 3,4-diaryl-3-pyrrolin-2-ones from tetramic acid triflates
A three-step approach to 4-aryl-3-phenyl-3-pyrrolin-2ones from a readily available tetramic acid is described. The introduction of different aryl groups to the 4-position of the ring system was accomplished utilizing Suzuki-Miyaura cross-coupling reactions of the corresponding tetramic acid triflate. This strategy was successfully employed in the first synthesis of the NH lactam analogue of rofecoxib.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 17924-92-4. HPLC of Formula: https://www.ambeed.com/products/17924-92-4.html.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem