Synthesis of poly(vinyl ether) optical plastics by cationic copolymerization of tricyclodecane vinyl ether with functionalized vinyl ethers

2012 ◽  
Vol 126 (S2) ◽  
pp. E307-E314 ◽  
Author(s):  
Takeshi Namikoshi ◽  
Tamotsu Hashimoto ◽  
Yuka Suzuki ◽  
Michio Urushisaki ◽  
Toshikazu Sakaguchi
2019 ◽  
Vol 10 (25) ◽  
pp. 3514-3524 ◽  
Author(s):  
Robert J. Kieber ◽  
Cuneyt Ozkardes ◽  
Natalie Sanchez ◽  
Justin G. Kennemur

Biomass-derived isosorbide (IS) was converted into a mono-glycal (i.e. vinyl ether) derivative (Gly-IS) to investigate its efficacy for cationic polymerization.


2015 ◽  
Vol 6 (8) ◽  
pp. 1236-1247 ◽  
Author(s):  
H. Bouchekif ◽  
A. I. Sulhami ◽  
R. D. Alghamdi ◽  
Y. Gnanou ◽  
N. Hadjichristidis

A series of novel, well-defined triblock and pentablock terpolymers of n-butyl vinyl ether (nBVE), 2-chloroethyl vinyl ether (CEVE) and tert-butyldimethylsilyl ethylene glycol vinyl ether (SiEGVE) were synthesized by sequential base-assisted living cationic polymerization.


Inorganics ◽  
2019 ◽  
Vol 7 (10) ◽  
pp. 121
Author(s):  
Takahashi ◽  
Shimbayashi ◽  
Fujita

The reaction of [(Cp*Ir)2(μ-dmpm)(μ-H)][OTf] (2) [Cp* = η5-C5Me5, dmpm = bis(dimethylphosphino)methane] with 2,3-dihydrofuran gives [(Cp*IrH)2(μ-dmpm){μ-(2,3-dihydrofuranyl)}][OTf] (3) in an isolated yield of 70% via the C–H bond activation at the 5-position of 2,3-dihydrofuran. Complex 3 is slowly converted into [(Cp*Ir)2(μ-dmpm)(μ-C=C(H)CH2CH2OH)][OTf] (4) quantitatively via the proton-mediated C–O bond activation. The reaction of 2 with ethyl vinyl ether gives [(Cp*Ir)2(μ-dmpm)(μ-CH=CH2)][OTf] (5) in the isolated yield of 64% via the successive activation of C–H and C–O bonds.


2005 ◽  
Vol 70 (9) ◽  
pp. 1411-1428 ◽  
Author(s):  
Petr Štěpánek ◽  
Ondřej Vích ◽  
Lukáš Werner ◽  
Ladislav Kniežo ◽  
Hana Dvořáková ◽  
...  

The stereoselectivity of cycloaddition of sugar-containing substituted 1-(thiazol-2-yl)but-2-en-1-ones 1 and vinyl ethers was studied using the achiral vinyl ether/chiral catalyst as well as the chiral vinyl ether/achiral catalyst combinations. It has been shown that Eu(fod)3-catalyzed cycloaddition of oxadienes 1a-1e with the chiral vinyl ethers 9 and 10 affords stereoselectively almost pure cycloadducts 11a-11e and 12a-12e, respectively. The obtained cycloadducts are suitable precursors for the synthesis of α-C-(1→3)-disaccharides, containing 2-deoxy-arabino-hexopyranose moiety of D- or L-configuration.


1970 ◽  
Vol 1 (1) ◽  
pp. 19-26 ◽  
Author(s):  
Tadashi Masuda ◽  
Toshinobu Higashimura ◽  
Seizo Okamura

2014 ◽  
Vol 71 (6) ◽  
pp. 1389-1402 ◽  
Author(s):  
Takeshi Namikoshi ◽  
Tamotsu Hashimoto ◽  
Yusuke Makino ◽  
Tsuguto Imaeda ◽  
Michio Urushisaki ◽  
...  
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