Synthesis and characterization of thiol‐acrylate hydrogels using a base‐catalyzed Michael addition for 3D cell culture applications

2020 ◽  
Vol 108 (5) ◽  
pp. 2294-2307 ◽  
Author(s):  
Anowar H. Khan ◽  
Jeffery K. Cook ◽  
Wayne J. Wortmann ◽  
Nathan D. Kersker ◽  
Asha Rao ◽  
...  
2019 ◽  
Vol 17 ◽  
pp. 441-446 ◽  
Author(s):  
Perumalsamy Balaji ◽  
Anbazhagan Murugadas ◽  
Sellathamby Shanmugaapriya ◽  
Mohammad Abdulkader Akbarsha

2015 ◽  
Vol 6 (10) ◽  
pp. 1805-1816 ◽  
Author(s):  
Vincent Ladmiral ◽  
Alexandre Charlot ◽  
Mona Semsarilar ◽  
Steven. P. Armes

Two amino acid methacrylates prepared via Michael addition are used as building blocks to prepare novel diblock copolymer nano-objects via polymerisation-induced self-assembly.


2020 ◽  
Vol 21 (3) ◽  
pp. 1254-1263
Author(s):  
Tian Li ◽  
Fei Huang ◽  
Diana Diaz-Dussan ◽  
Jianyang Zhao ◽  
Shruti Srinivas ◽  
...  

2014 ◽  
Vol 26 (29) ◽  
pp. 4919-4919 ◽  
Author(s):  
Zhenzhen Liu ◽  
Qiuning Lin ◽  
Yun Sun ◽  
Tao Liu ◽  
Chunyan Bao ◽  
...  

2017 ◽  
Vol 4 (4) ◽  
pp. 51 ◽  
Author(s):  
Dominik Egger ◽  
Monica Fischer ◽  
Andreas Clementi ◽  
Volker Ribitsch ◽  
Jan Hansmann ◽  
...  

2019 ◽  
Vol 15 ◽  
pp. 1116-1128 ◽  
Author(s):  
Shahien Shahsavari ◽  
Dhananjani N A M Eriyagama ◽  
Bhaskar Halami ◽  
Vagarshak Begoyan ◽  
Marina Tanasova ◽  
...  

Solid-phase synthesis of electrophilic oligodeoxynucleotides (ODNs) was achieved using dimethyl-Dmoc (dM-Dmoc) as amino protecting group. Due to the high steric hindrance of the 2-(propan-2-ylidene)-1,3-dithiane side product from deprotection, the use of excess nucleophilic scavengers such as aniline to prevent Michael addition of the side product to the deprotected ODN during ODN cleavage and deprotection was no longer needed. The improved technology was demonstrated by the synthesis and characterization of five ODNs including three modified ones. The modified ODNs contained the electrophilic groups ethyl ester, α-chloroamide, and thioester. Using the technology, the sensitive groups can be installed at any location within the ODN sequences without using any sequence- or functionality-specific conditions and procedures.


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