Some scientific research about 5264-35-7

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 5264-35-7, and how the biochemistry of the body works.Electric Literature of 5264-35-7

Electric Literature of 5264-35-7, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.5264-35-7, Name is 5-Methoxy-3,4-dihydro-2H-pyrrole, molecular formula is C5H9NO. In a Article£¬once mentioned of 5264-35-7

sp3 C-H bond arylation directed by amidine protecting group: alpha-arylation of pyrrolidines and piperidines

A new ruthenium-catalyzed direct sp3 C-H to C-C bond transformation is disclosed. Specifically, a method for the alpha-arylation of cyclic amines, containing either permanent (pyridine, pyrimidine) or removable (amidine) directing groups, is described. This cross-coupling reaction involves heating amine substrates with arylboronate ester at 150 C in a ketone solvent with a catalytic amount of ruthenium carbonyl [Ru3(CO)12]. Arylboronate esters containing either electron-withdrawing or electron-donating substituents could be efficiently coupled. Heteroarene boronates were also effective donors. Copyright

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 5264-35-7, and how the biochemistry of the body works.Electric Literature of 5264-35-7

Reference£º
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem