scholarly journals Poly(ethylene glycol) as reaction medium for mild Mizoroki–Heck reaction in a ball-mill

2012 ◽  
Vol 48 (96) ◽  
pp. 11778 ◽  
Author(s):  
Valérie Declerck ◽  
Evelina Colacino ◽  
Xavier Bantreil ◽  
Jean Martinez ◽  
Frédéric Lamaty
ChemInform ◽  
2013 ◽  
Vol 44 (14) ◽  
pp. no-no
Author(s):  
Valerie Declerck ◽  
Evelina Colacino ◽  
Xavier Bantreil ◽  
Jean Martinez ◽  
Frederic Lamaty

2006 ◽  
Vol 59 (4) ◽  
pp. 260 ◽  
Author(s):  
Mohamed Makha ◽  
Colin L. Raston ◽  
Alexandre N. Sobolev

p-Phenylcalix[4]arene is formed directly from p-phenylphenol in 66% yield (50% isolated yield) using poly(ethylene glycol) as the reaction medium, with crystallization of the pure cavitand from toluene mediated by p-carborane. The solid-state structure comprises interlocking columnar arrays.


2007 ◽  
Vol 79 (9) ◽  
pp. 1481-1489 ◽  
Author(s):  
Yasuhiro Uozumi

A novel homochiral phosphine ligand, (3R,9aS)[2-aryl-3-(2-diphenylphosphino)phenyl]tetrahydro-1H-imidazo[1,5-a]indole-1-one, was designed, prepared, and anchored onto an amphiphilic polystyrene-poly(ethylene glycol) copolymer (PS-PEG) resin. Catalytic asymmetric substitution of a racemic mixture of cycloalkenyl esters with carbon, nitrogen, and oxygen nucleophiles was achieved in water as the single reaction medium under heterogeneous conditions by using the PS-PEG resin-supported palladium-imidazoindole phosphine complex to give optically active substituted cycloalkenes with up to 99 % ee.


2009 ◽  
Vol 62 (8) ◽  
pp. 917 ◽  
Author(s):  
Jing-Lun Wang ◽  
Liang-Nian He ◽  
Xiao-Yong Dou ◽  
Fang Wu

Poly(ethylene glycol) (PEG) in this work proved to be an efficient reaction medium for the reaction of vicinal halohydrin with carbon dioxide in the presence of a base to synthesise cyclic carbonates. Notably, PEG-400 as an environmentally friendly solvent exhibits a unique influence on reactivity compared with conventional organic solvents. Various cyclic carbonates were prepared in high yield employing this protocol. The process presented here has potential applications in the industrial production of cyclic carbonates because of its simplicity, cost benefits, ready availability of starting materials, and mild reaction conditions.


2002 ◽  
Vol 4 (25) ◽  
pp. 4399-4401 ◽  
Author(s):  
S. Chandrasekhar ◽  
Ch. Narsihmulu ◽  
S. Shameem Sultana ◽  
N. Ramakrishna Reddy

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