In 2019 J MASS SPECTROM published article about BOND ACTIVATION; METAL-IONS; DECARBOXYLATION; MECHANISMS in [Piacentino, Elettra L.; Rodriguez, Edwin; Parker, Kevin; Gilbert, Thomas M.; Ryzhov, Victor] Northern Illinois Univ, Dept Chem & Biochem, De Kalb, IL 60115 USA; [O’Hair, Richard A. J.] Univ Melbourne, Bio Inst 21, Melbourne, Vic 3010, Australia; [O’Hair, Richard A. J.] Univ Melbourne, Sch Chem, Melbourne, Vic 3010, Australia in 2019, Cited 27. The Name is 4-Methoxybenzyl acetate. Through research, I have a further understanding and discovery of 104-21-2. Application In Synthesis of 4-Methoxybenzyl acetate
Gas-phase C?C coupling reactions mediated by Ni (II) complexes were studied using a linear quadrupole ion trap mass spectrometer. Ternary nickel cationic carboxylate complexes, [(phen)Ni (OOCR1)](+) (where phen = 1,10-phenanthroline), were formed by electrospray ionization. Upon collision-induced dissociation (CID), they extrude CO2 forming the organometallic cation [(phen)Ni(R-1)](+), which undergoes gas-phase ion-molecule reactions (IMR) with acetate esters CH3COOR2 to yield the acetate complex [(phen)Ni (OOCCH3)](+) and a C?C coupling product R-1-R-2. These Ni(II)/phenanthroline-mediated coupling reactions can be performed with a variety of carbon substituents R-1 and R-2 (sp(3), sp(2), or aromatic), some of them functionalized. Reaction rates do not seem to be strongly dependent on the nature of the substituents, as sp(3)-sp(3) or sp(2)-sp(2) coupling reactions proceed rapidly. Experimental results are supported by density functional theory calculations, which provide insights into the energetics associated with the C?C bond coupling step.
About 4-Methoxybenzyl acetate, If you have any questions, you can contact Piacentino, EL; Rodriguez, E; Parker, K; Gilbert, TM; O’Hair, RAJ; Ryzhov, V or concate me.. Application In Synthesis of 4-Methoxybenzyl acetate
Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem