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The growing applications of click chemistry

Chem. Soc. Rev., 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
John E, Moses, Adam D, Moorhouse
openaire   +2 more sources

Click-Chemistry in Biocatalysis

Current Organic Chemistry, 2013
Peer ...
openaire   +2 more sources

Ultrafast Click Chemistry with Fluorosydnones

Angewandte Chemie International Edition, 2016
AbstractWe report the synthesis and reactivity of 4‐fluorosydnones, a unique class of mesoionic dipoles displaying exquisite reactivity towards both copper‐catalyzed and strain‐promoted cycloaddition reactions with alkynes. Synthetic access to these new mesoionic compounds was granted by electrophilic fluorination of σ‐sydnone PdII precursors in the ...
Liu, Hui   +13 more
openaire   +5 more sources

Click chemistry in sphingolipid research

Chemistry and Physics of Lipids, 2018
The term "click chemistry" was firstly coined by K. B. Sharpless in 2001 to refer to reactions that are high yielding, wide in scope, produce only easily removable byproducts and are stereospecific and simple to perform. Since then, this concept has been further developed and a large number of chemical reactions that fulfil totally or partially these ...
Eduardo Izquierdo, Antonio Delgado
openaire   +2 more sources

Light-Triggered Click Chemistry

Chemical Reviews, 2020
The merging of click chemistry with discrete photochemical processes has led to the creation of a new class of click reactions, collectively known as photoclick chemistry. These light-triggered click reactions allow the synthesis of diverse organic structures in a rapid and precise manner under mild conditions.
Gangam Srikanth Kumar, Qing Lin
openaire   +2 more sources

Protein Iodination by Click Chemistry

ChemBioChem, 2009
AbstractTwo steps to click iodine: We have developed a two‐step reaction for protein iodination using click chemistry. With this method, which is summarized in the scheme, covalent attachment of a stable iodine‐containing aromatic azide moiety to an alkyne‐containing protein was achieved.magnified ...
Dong, S., Moroder, L., Budisa, N.
openaire   +3 more sources

Click Here for Better Chemistry

New England Journal of Medicine, 2022
Brian M, Zeglis, Jason S, Lewis
openaire   +2 more sources

Accelerated SuFEx Click Chemistry For Modular Synthesis**

Angewandte Chemie - International Edition, 2022
Christopher Smedley   +2 more
exaly  

Macromolecular engineering in functional polymers via ‘click chemistry’ using triazolinedione derivatives

Progress in Polymer Science, 2021
Prantik Mondal   +2 more
exaly  

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