epoxy acid
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2021 ◽  
Author(s):  
Camille Bakkali-Hassani ◽  
Quentin-Arthur Poutrel ◽  
Jakob Langenbach ◽  
Sélène Chappuis ◽  
Jonny J. Blaker ◽  
...  

2020 ◽  
Vol 11 (33) ◽  
pp. 5327-5338 ◽  
Author(s):  
Quentin-Arthur Poutrel ◽  
Jonny J. Blaker ◽  
Constantinos Soutis ◽  
François Tournilhac ◽  
Matthieu Gresil

Vitrimers with 1 : 1 to 2 : 1 epoxy/acid ratio and TBD show increased stiffness and gradual transition from an exchangeable to non-exchangeable network.


Soft Matter ◽  
2020 ◽  
Vol 16 (6) ◽  
pp. 1668-1677 ◽  
Author(s):  
Honggeng Li ◽  
Biao Zhang ◽  
Kai Yu ◽  
Chao Yuan ◽  
Cong Zhou ◽  
...  

The effects of particle size, temperature, time, and pressure on the mechanical properties of regenerated epoxy-acid vitrimers were investigated, which helped to refine the vitrimer reprocessing condition parameter toolbox.


2018 ◽  
Vol 5 (23) ◽  
pp. 3402-3405 ◽  
Author(s):  
Jinhong Chen ◽  
Junfang Li ◽  
Longqing Zhu ◽  
Xue Peng ◽  
Yiyue Feng ◽  
...  

Total synthesis and structure revision of chrysamide B are described, the strategy features a convergent assembly of the chiral piperazine core and epoxy-acid.


2017 ◽  
Vol 58 (1) ◽  
pp. 28-36 ◽  
Author(s):  
Christopher Thurber ◽  
Liangliang Gu ◽  
Jason C. Myers ◽  
Timothy P. Lodge ◽  
Christopher W. Macosko

RSC Advances ◽  
2016 ◽  
Vol 6 (91) ◽  
pp. 88647-88655 ◽  
Author(s):  
F. I. Altuna ◽  
C. E. Hoppe ◽  
R. J. J. Williams

The shape of epoxy–acid based vitrimers can be changed either temporarily or permanently by selecting the appropriate thermal treatment.


ChemInform ◽  
2010 ◽  
Vol 41 (3) ◽  
Author(s):  
Jose M. Concellon ◽  
Pablo L. Bernad ◽  
Humberto Rodriguez-Solla ◽  
Pamela Diaz
Keyword(s):  

2009 ◽  
Vol 351 (13) ◽  
pp. 2178-2184 ◽  
Author(s):  
José M. Concellón ◽  
Pablo L. Bernad ◽  
Humberto Rodríguez-Solla ◽  
Pamela Díaz
Keyword(s):  

2008 ◽  
Vol 63 (5) ◽  
pp. 595-599 ◽  
Author(s):  
Braulio M. Fraga ◽  
Carlo Bressa ◽  
Concepción Fernández ◽  
Pedro González ◽  
Ricardo Guillermo ◽  
...  

A phytochemical study of Sideritis infernalis led to the isolation of the new nor-diterpene adejone (17-nor-7α,18-dihydroxy-ent-kaur-16-one). The biosynthesis of this compound implies the decarboxylation of an epoxy-acid as the last step. In addition, three diterpenes with an ent-kaurene skeleton, episideridiol, candicandiol 7α-monoacetate and candidiol 15α-monoacetate, have been isolated from S. candicans for the first time in nature.


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