نتایج جستجو برای: click chemistry

تعداد نتایج: 118439  

Journal: :Electrochemistry Communications 2019

Journal: :Proceedings of the National Academy of Sciences 2010

2009
Cole A. DeForest Brian D. Polizzotti Kristi S. Anseth

Click chemistry provides extremely selective and orthogonal reactions that proceed with high efficiency and under a variety of mild conditions, the most common example being the copper(I)-catalysed reaction of azides with alkynes1,2. While the versatility of click reactions has been broadly exploited3–5, a major limitation is the intrinsic toxicity of the synthetic schemes and the inability to ...

Journal: :Chemical communications 2009
Beth M Cooper Delphine Chan-Seng Debasis Samanta Xiongfei Zhang Sangram Parelkar Todd Emrick

Phosphorylcholine (PC)-substitution on aliphatic polyesters is accomplished by click chemistry with PC-substituted azides.

Journal: :Molecules 2011
Dieter Verzele Sara Figaroli Annemieke Madder

We present three versatile solid-supported scaffold building blocks based on the (deoxy)cholic acid framework and decorated with handles for further derivatization by modern ligation techniques such as click chemistry, Staudinger ligation or native chemical ligation. Straightforward procedures are presented for the synthesis and analysis of the steroid constructs. These building blocks offer a ...

2015
Roberto Romeo Caterina Carnovale Salvatore V Giofrè Maria A Chiacchio Adriana Garozzo Emanuele Amata Giovanni Romeo Ugo Chiacchio

A novel series of 2'-oxa-3'-aza-4'a-carbanucleosides, featured with a triazole linker at the 5'-position, has been developed by exploiting a click chemistry reaction of 5'-azido-2'-oxa-3'-aza-4'a-carbanucleosides with substituted alkynes. Biological tests indicate an antitumor activity for the synthesized compounds: most of them inhibit cell proliferation of Vero, BS-C-1, HEp-2, MDCK, and HFF c...

Journal: :Quarterly reviews of biophysics 2015
Afaf H El-Sagheer Tom Brown

We describe the development of a chemical process based on the CuAAC reaction (click chemistry) to ligate DNA strands and produce an unnatural triazole backbone linkage. The chemical reaction is templated by a complementary DNA splint which accelerates the reaction and provides the required specificity. The resultant 1,4-triazole linkage is read through by DNA and RNA polymerases and is biocomp...

Journal: :SynOpen 2023

Abstract Triazole-based compounds possess a broad range of activity and can be synthesized using click chemistry. Many new chemotherapeutic agents have been developed in recent years by exploiting chemistry these are covered this review.

Journal: :Chemical Communications 2021

A thiol-epoxy click chemistry reaction is used to introduce thiol groups on magnetic nanogels for the attachment of Au nanorods.

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