Microwave Accelerated Polymerization of 2-Phenyl-2-oxazoline.
Sinnwell S and Ritter H.
Macromolecular Rapid Communications, 26(3), 160-163 (2005)
Andrew M Kelly et al.
Macromolecular rapid communications, 32(22), 1815-1819 (2011-09-21)
A 32-membered library of poly(2-oxazoline)-based hydrogels of the composition pEtOx(m) -pPhOx(n) -pPBO(q) (m/n = 150/0, 100/50, 50/100, and 0/150; q = 1.5-30) was prepared from 2-ethyl- (EtOx), 2-phenyl-2-oxazoline (PhOx), and phenylene-1,3-bis-(2-oxazoline) (PBO). The polymerizations were performed from ground monomer mixtures...
One-pot synthesis of 2-phenyl-2-oxazoline-containing quasi-diblock copoly (2-oxazoline) s under microwave irradiation.
Hoogenboom R, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 45(3), 416-422 (2007)
Robert A Gossage et al.
Dalton transactions (Cambridge, England : 2003), (23)(23), 3115-3122 (2008-06-04)
The treatment of cold ( approximately 3 degrees C) methanolic solutions of Li(2)PdCl(4) with two equivalents of 2-phenyl-2-oxazoline (Phox) results in the isolation of [PdCl(2)(Phox)(2)] (3). This complex undergoes remarkably slow isomerisation (CHCl(3)-d) at room temperature to a corresponding thermodynamic...
Indira Fabre et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(23), 7595-7604 (2013-04-19)
The activation of the C-H bond of 1-phenylpyrazole (2) and 2-phenyl-2-oxazoline (3) by [Ru(OAc)2(p-cymene)] is an autocatalytic process catalyzed by the co-product HOAc. The reactions are indeed faster in the presence of acetic acid and water but slower in the...