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Agribusiness, EarlyView.Abstract The Russian invasion of Ukraine in February 2022 had profound consequences for the global economy. As both countries are major commodity exporters, the food value chain was also affected. This study investigates the impact of the invasion on stock prices, profitability and sentiments of agribusinesses along the food supply chain by using an ...
Julia Höhler +2 more
wiley +1 more source
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A laccase-catalysed tyrosine click reaction
Organic & Biomolecular Chemistry, 2020The tyrosine click reaction of peptides/proteins with the tyrosine modification reagent, N-methyl luminol, was catalysed by a laccase in the presence of molecular oxygen (O2) at 37 °C.
Shinichi Sato +2 more
openaire +3 more sources
Efficient DNA Click Reaction Replaces Enzymatic Ligation
Bioconjugate Chemistry, 2019 We report a chemical DNA-DNA ligation method based on copper-catalyzed azide-alkyne cycloaddition (CuAAC). We demonstrate that ion addition dramatically influences the efficiency of the so-called click reaction. Even without any further additions, such as typically splint oligonucleotides for preorganization, the "click ligation" yields up to ∼83 ...
Michael Kollaschinski +5 more
openaire +3 more sources
Cu-Catalyzed Click Reaction in Carbohydrate Chemistry
Chemical Reviews, 2016Cu(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition (CuAAC), popularly known as the "click reaction", serves as the most potent and highly dependable tool for facile construction of simple to complex architectures at the molecular level. Click-knitted threads of two exclusively different molecular entities have created some really interesting ...
Vinod K, Tiwari +5 more
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Dynamic Enamine-one Bond Based Vitrimer via Amino-yne Click Reaction.
ACS Macro Letters, 2021Here, we report the fabrication of a dynamic enamine-one bond based vitrimer through amino-yne click chemistry. In contrast to amine-acetoacetate condensation, the amino-yne click reaction yields a dynamic enamine-one motif that is composed of cis/trans (
Xinru Guo +6 more
semanticscholar +1 more source
Current Organic Chemistry, 2016
The Diels-Alder reactions can be classified as click reactions because of their simplicity and high yields. The Diels-Alder click reactions have been used for the preparation of complex macromolecules, such as hydrogels and polymers and also for labeling of various biological targets.
Dajana Ga.so-Soka.c, Marija Stivojevi.c
+5 more sources
The Diels-Alder reactions can be classified as click reactions because of their simplicity and high yields. The Diels-Alder click reactions have been used for the preparation of complex macromolecules, such as hydrogels and polymers and also for labeling of various biological targets.
Dajana Ga.so-Soka.c, Marija Stivojevi.c
+5 more sources
Chem. Soc. Rev., 2010
Fluorogenic Cu(I)-catalyzed alkyne-azide cycloaddition (CuAAC) reactions have emerged as a powerful tool for bioconjugation, materials science, organic synthesis and drug discovery. This review highlights the design of the recent development of fluorogenic CuAAC reactions as well as their applications.
Céline, Le Droumaguet +2 more
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Fluorogenic Cu(I)-catalyzed alkyne-azide cycloaddition (CuAAC) reactions have emerged as a powerful tool for bioconjugation, materials science, organic synthesis and drug discovery. This review highlights the design of the recent development of fluorogenic CuAAC reactions as well as their applications.
Céline, Le Droumaguet +2 more
openaire +2 more sources
, 2020
The thiol–ene click reaction to prepare biobased polyols is a strategy to promote the green and environmental protection of polyurethane.
Yujing Hu +3 more
semanticscholar +1 more source
The thiol–ene click reaction to prepare biobased polyols is a strategy to promote the green and environmental protection of polyurethane.
Yujing Hu +3 more
semanticscholar +1 more source
Angewandte Chemie International Edition, 2013
AbstractSpatial and temporal control over chemical and biological processes, both in terms of “tuning” products and providing site‐specific control, is one of the most exciting and rapidly developing areas of modern science. For synthetic chemists, the challenge is to discover and develop selective and efficient reactions capable of generating useful ...
Mehmet Atilla, Tasdelen, Yusuf, Yagci
openaire +2 more sources
AbstractSpatial and temporal control over chemical and biological processes, both in terms of “tuning” products and providing site‐specific control, is one of the most exciting and rapidly developing areas of modern science. For synthetic chemists, the challenge is to discover and develop selective and efficient reactions capable of generating useful ...
Mehmet Atilla, Tasdelen, Yusuf, Yagci
openaire +2 more sources