scholarly journals A Model for Late-Stage Modification of Polyurethane Dendrimers Using Thiol–Ene Click Chemistry

ACS Omega ◽  
2021 ◽  
Author(s):  
Dhruba P. Poudel ◽  
Richard T. Taylor
Keyword(s):  
2021 ◽  
Author(s):  
Dhruba Poudel ◽  
Richard Taylor

Protecting group free, one-pot multicomponent Curtius reaction was utilized to afford diurethane G-1 dendron. In our synthetic approach, G-1 dendron can undergo late-stage modification using thiol-ene click reaction, which was then attached to the core to furnish a dendrimer. In another approach, the G-1 dendron was attached to the core and so formed dendrimer was surface functionalized using thiol-ene click chemistry. Either way, we can synthesize the dendrimer.


2018 ◽  
Vol 140 (8) ◽  
pp. 2919-2925 ◽  
Author(s):  
Zilei Liu ◽  
Jie Li ◽  
Suhua Li ◽  
Gencheng Li ◽  
K. Barry Sharpless ◽  
...  
Keyword(s):  

2019 ◽  
Author(s):  
rahul upadhyay ◽  
Rahul Kumar ◽  
Rohit Rana ◽  
Onkar S. Nayal ◽  
Sushil K. Maurya

2021 ◽  
Author(s):  
Dhruba Poudel ◽  
Richard Taylor

Protecting group free, one-pot multicomponent Curtius reaction was utilized to afford diurethane G-1 dendron. In our synthetic approach, G-1 dendron can undergo late-stage modification using thiol-ene click reaction, which was then attached to the core to furnish a dendrimer. In another approach, the G-1 dendron was attached to the core and so formed dendrimer was surface functionalized using thiol-ene click chemistry. Either way, we can synthesize the dendrimer.


2020 ◽  
Vol 21 (11) ◽  
pp. 3964
Author(s):  
Nile S. Abularrage ◽  
Brian J. Levandowski ◽  
Ronald T. Raines

4H-Pyrazoles are emerging scaffolds for “click” chemistry. Late-stage fluorination with Selectfluor® is found to provide a reliable route to 4-fluoro-4-methyl-4H-pyrazoles. 4-Fluoro-4-methyl-3,5-diphenyl-4H-pyrazole (MFP) manifested 7-fold lower Diels–Alder reactivity than did 4,4-difluoro-3,5-diphenyl-4H-pyrazole (DFP), but higher stability in the presence of biological nucleophiles. Calculations indicate that a large decrease in the hyperconjugative antiaromaticity in MFP relative to DFP does not lead to a large loss in Diels–Alder reactivity because the ground-state structure of MFP avoids hyperconjugative antiaromaticity by distorting into an envelope-like conformation like that in the Diels–Alder transition state. This predistortion enhances the reactivity of MFP and offsets the decrease in reactivity from the diminished hyperconjugative antiaromaticity.


Author(s):  
Qinheng Zheng ◽  
Hongtao Xu ◽  
Hua Wang ◽  
Wen-Ge Han Du ◽  
Nan Wang ◽  
...  

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