Gradient copolymers of ε‐caprolactone and δ‐valerolactone via solvent‐free ring‐opening copolymerization with a pyridyl‐urea/ MTBD system

2020 ◽  
Vol 58 (15) ◽  
pp. 2108-2115
Author(s):  
Rui Feng ◽  
Suyun Jie ◽  
Pierre Braunstein ◽  
Bo‐Geng Li
2020 ◽  
Vol 22 (7) ◽  
pp. 2197-2202 ◽  
Author(s):  
Simon P. Bassett ◽  
Andrew D. Russell ◽  
Paul McKeown ◽  
Isabel Robinson ◽  
Thomas R. Forder ◽  
...  

A stereoselective, solvent-free ring-opening polymerisation (ROP) of lactide (LA) in supercritical carbon dioxide (scCO2) is reported for the first time.


2019 ◽  
Vol 58 (37) ◽  
pp. 17255-17265 ◽  
Author(s):  
Shiyu Chen ◽  
Manoj Pudukudy ◽  
Zhongxiao Yue ◽  
Heng Zhang ◽  
Yunfei Zhi ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-6 ◽  
Author(s):  
Mohamed A. Said ◽  
Wagdy M. Eldehna ◽  
Hazem A. Ghabbour ◽  
Maha M. Kabil ◽  
Nasser S. Al-shakliah ◽  
...  

Certain Biginelli pyrimidines with ester substitution in C5 were subjected to unexpected ring opening upon solvent-free reaction with hydrazine hydrate to give three products: pyrazole, arylidenehydrazines, and urea/thiourea, respectively. The nonisolable carbohydrazide intermediates are formed firstly followed by the intermolecular nucleophilic attack of terminal amino group of hydrazide function on sp2 C6 rather than the sp3 C4 to give the ring adduct which was produced as a final product.


2019 ◽  
Author(s):  
Kesatebrhan Haile Asressu ◽  
Cheng-Chung Wang

Sialic acid-containing glycans are found in different sialic acid forms and a variety of glycosidic linkages in biologically active glycoconjugates. Hence, the preparation of suitably protected sialyl building blocks requires high attention in order to access glycans in pure form. In this line, various C-5 substituted 2,7-anhydrosialic acid derivatives bearing both electron donating and withdrawing protecting groups were synthesized and subjected to different Lewis acid-catalyzed solvent free ring opening reactions at room temperature in the presence of acetic anhydride. Among the various Lewis acids tested, the desired acetolysized products were obtained in moderate yields under a tin(IV) chloride catalysis system. Our methodology can be extended to regioselective protecting group installation and manipulation towards a number of thiosialoside and halide donors.


2017 ◽  
Vol 58 (10) ◽  
pp. 977-980 ◽  
Author(s):  
Nelson Nuñez-Dallos ◽  
Andrés F. Posada ◽  
John Hurtado

2008 ◽  
pp. 1293 ◽  
Author(s):  
Amanda J. Chmura ◽  
Matthew G. Davidson ◽  
Catherine J. Frankis ◽  
Matthew D. Jones ◽  
Matthew D. Lunn

2016 ◽  
Vol 37 (22) ◽  
pp. 1832-1836 ◽  
Author(s):  
Cherif Larabi ◽  
Kai C. Szeto ◽  
Yassine Bouhoute ◽  
Marc O. Charlin ◽  
Nicolas Merle ◽  
...  

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