Rapid Synthesis of Triazole-Modified Resveratrol Analogues via Click Chemistry

2006 ◽  
Vol 49 (2) ◽  
pp. 467-470 ◽  
Author(s):  
Francesca Pagliai ◽  
Tracey Pirali ◽  
Erika Del Grosso ◽  
Riccardo Di Brisco ◽  
Gian Cesare Tron ◽  
...  
Keyword(s):  
Click Chemistry ◽  
Rapid Synthesis ◽  
Resveratrol Analogues

A “Click Chemistry Platform” for the Rapid Synthesis of Bispecific Molecules for Inducing Protein Degradation

2017 ◽  
Vol 61 (2) ◽  
pp. 453-461 ◽  
Author(s):  
Ryan P. Wurz ◽  
Ken Dellamaggiore ◽  
Hannah Dou ◽  
Noelle Javier ◽  
Mei-Chu Lo ◽  
...  
Keyword(s):  
Protein Degradation ◽  
Click Chemistry ◽  
Rapid Synthesis

Rapid synthesis of flavone-based monoamine oxidase (MAO) inhibitors targeting two active sites using click chemistry

2016 ◽  
Vol 89 (1) ◽  
pp. 141-151 ◽  
Author(s):  
Wei Zhen Jia ◽  
Feng Cheng ◽  
Yin Jun Zhang ◽  
Jin Yan Ge ◽  
Shao Q. Yao ◽  
...  
Keyword(s):  
Monoamine Oxidase ◽  
Click Chemistry ◽  
Active Sites ◽  
Mao Inhibitors ◽  
Rapid Synthesis

Functionalized ionic liquids with highly polar polyhydroxylated appendages and their rapid synthesis via thiol-ene click chemistry

2011 ◽  
Vol 52 (40) ◽  
pp. 5173-5175 ◽  
Author(s):  
Richard A. O’Brien ◽  
Arsalan Mirjafari ◽  
Vijayakumari Jajam ◽  
Erin N. Capley ◽  
Alexandra C. Stenson ◽  
...  
Keyword(s):  
Ionic Liquids ◽  
Click Chemistry ◽  
Rapid Synthesis

Rapid Synthesis of Silk-Like Polymers Facilitated by Microwave Irradiation and Click Chemistry

2020 ◽  
Author(s):  
Amrita Sarkar ◽  
Cody Edson ◽  
Ding Tian ◽  
Tanner D. Fink ◽  
Katherine Cianciotti ◽  
...  
Keyword(s):  
Microwave Irradiation ◽  
Click Chemistry ◽  
Rapid Synthesis

Rapid assembly of potent type II dehydroquinase inhibitorsvia “Click” chemistry

MedChemComm ◽  
2010 ◽  
Vol 1 (4) ◽  
pp. 271-275 ◽  
Author(s):  
Anh Thu Tran ◽  
Katie M. Cergol ◽  
Warwick J. Britton ◽  
Syed Ali Imran Bokhari ◽  
Musadiq Ibrahim ◽  
...  
Keyword(s):  
Click Chemistry ◽  
Type Ii ◽  
Rapid Synthesis ◽  
Type Ii Dehydroquinase

The rapid synthesis of a library of potent type II dehydroquinase inhibitors is described. Inhibitors were prepared via a key quinate-derived ene-yne intermediate using Cu(i)-catalysed azide-alkyne cycloaddition (CuAAC) chemistry with a variety of aryl- and heteroaryl-azides.

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