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Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 06/2019, Volume 57, Issue 12, pp. 1358 - 1364
ABSTRACT A route from naturally occurring myo‐inositol to hydroxyl‐bearing polyurethanes has been developed. The diol prepared from the bis‐acetalization of... 
deprotection | polyurethane | renewable resources | acetal | step‐growth polymerization | myo‐inositol | Isocyanates | Inositol | Hydroxides | Hydrogen | Cyclohexane | Polymerization | Nuclear magnetic resonance spectroscopy | Polyurethanes | Polyurethane resins | Hydrogen bonds | Chains | Glass transition temperature | Diisocyanates | Hydroxyl groups | Bearing
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 09/2013, Volume 51, Issue 18, pp. 3867 - 3872
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 11/2016, Volume 54, Issue 21, pp. 3436 - 3443
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 11/2019, Volume 57, Issue 21, pp. 2145 - 2148
A polymer containing a zwitterionic form in the main chain was synthesized by the polyaddition of a bifunctional cyclic amidine with diisothiocyanate. The ion... 
diisothiocyanate | cyclic amidine | step‐growth polymerization | thermal properties | polyelectrolytes | Lithium | Lithium chlorides | Polymers | Polymeric films
Journal Article
Molecules, ISSN 1420-3049, 12/2016, Volume 21, Issue 12, p. 1720
n/a
Journal Article
Kobunshi Ronbunshu, ISSN 0386-2186, 05/2015, Volume 72, Issue 5, pp. 232 - 242
The target of the studies described herein is the development of high performance polymers from monosaccharides and myo-inositol. These naturally occurring... 
Synthesis | Utilization | Feasibility | Derivatives | Polymers | Polyols | Monomers | Monosaccharides
Journal Article
Kobunshi Ronbunshu, ISSN 0386-2186, 05/2015, Volume 72, Issue 5, pp. 232 - 242
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 07/2019, Volume 57, Issue 14, p. 1564
Oligo(spiroorthocarbonate)s 1, which were synthesized by the polycondensation of pentaerythritol derivatives with tetraethylorthocarbonate, were employed as... 
Crosslinked polymers
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 11/2017, Volume 55, Issue 22, pp. 3798 - 3803
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 07/2019, Volume 57, Issue 14, pp. 1564 - 1568
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 04/2019, Volume 57, Issue 7, pp. 792 - 798
ABSTRACT A series of soluble oligo(spiroorthocarbonate)s (OSOCs) were synthesized by polycondensation of tetraethylorthocarbonate with pentaerythritol... 
spiroorthocarbonates | polycondensation | pentaerythritol | spiropolymers | POLYMER SCIENCE | Synthesis | Derivatives | NMR spectroscopy | Aliphatic compounds
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 08/2019, Volume 57, Issue 16, pp. 1723 - 1729
ABSTRACT Radical ring‐opening polymerization of 1,1‐dicyano‐2‐vinylcyclopropane 1 was performed in benzonitrile to find the corresponding homopolymer 2 soluble... 
radical ring‐opening polymerization | vinyl cyclopropane | radical copolymerization | POLYMER SCIENCE | VINYLCYCLOPROPANE | radical ring-opening polymerization | SUBSTITUTED CYCLOPROPANES | Polymerization | Nitriles | Cyclopropane compounds | Solvents | Copolymers | Crosslinking | Copolymerization | Glass transition temperature | Benzonitrile
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 04/2019, Volume 57, Issue 7, p. 792
A series of soluble oligo(spiroorthocarbonate)s (OSOCs) were synthesized by polycondensation of tetraethylorthocarbonate with pentaerythritol derivatives. The... 
Analysis | Pentaerythritol | Nuclear magnetic resonance spectroscopy
Journal Article
International journal of molecular sciences, ISSN 1661-6596, 10/2018, Volume 19, Issue 10, p. 2979
The poor prognosis of pancreatic cancer requires the development of more effective therapy. CD147 expresses in pancreatic cancer with high incidence and has a... 
combination therapy | pancreatic cancer | gemcitabine | radioimmunotherapy | extracellular matrix metalloproteinase inducer
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 01/2015, Volume 33, Issue 3_suppl, pp. 163 - 163
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 08/2018, Volume 56, Issue 15, pp. 1743 - 1748
ABSTRACT Two stereoisomeric trimethacrylates, T1 and T2, which share a common adamantane‐like rigid core, were synthesized from naturally occurring... 
networked polymer | renewable resources | cyclopolymerization | myo‐inositol | radical polymerization | myo-inositol | POLYMERS | DESIGN | POLYMER SCIENCE | MONOMER | RATIO | SCYLLO-INOSITOL | RING FORMATION | SEQUENCE | SCAFFOLD | Polymerization | Inositol | Hydroxides | Polymers | Precursors | Crosslinking | Chemical synthesis | Thermal stability | Hydroxyl groups
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 11/2016, Volume 54, Issue 21, pp. 3436 - 3443
ABSTRACT A rigid diamine was synthesized from myo‐inositol, a naturally occurring cyclic hexaol, and used as a monomer to synthesize polyamides. myo‐Inositol... 
polycondensation | diamine | polyamide | renewable resources | myo‐inositol | myo-inositol | HIGH-PERFORMANCE | POLYESTERS | INOSITOL DERIVATIVES | POLYMER SCIENCE | ACID | BUILDING-BLOCKS | POLYMERIZATION | ISOSORBIDE | BIODEGRADABLE POLYMERS | Inositol | Usage | Polyamides | Polyamide resins | Diamines | Dicarboxylic acids | Derivation | Chains | Glass transition temperature | Monomers | Diols
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2013, Volume 8, Issue 9, p. e72802
Journal Article
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 04/2018, Volume 56, Issue 7, pp. 783 - 788
ABSTRACT Radical ring‐opening polyaddition of bifunctional vinyloxirane with multifunctional thiols was investigated. The polyaddition proceeded smoothly via... 
networked polysulfide | radical ring‐opening polyaddition | vinyloxirane | multifunctional thiol | volume change | radical ring-opening polyaddition | MONOMERS | POLYMER SCIENCE | CYCLIC ALLYLIC SULFIDES | 2-PHENYL-3-VINYLOXIRANE DERIVATIVES | RING-OPENING POLYMERIZATION | Thiols | Oxirane | Thermodynamic properties
Journal Article
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