Results 21 to 30 of about 28,542 (223)

The mode of action of isocyanide in three aquatic organisms, Balanus amphitrite, Bugula neritina and Danio rerio. [PDF]

open access: yesPLoS ONE, 2012
Isocyanide is a potential antifouling compound in marine environments. In this study, we investigated its mode of action in three aquatic organisms. Two of them, the bryozoan Bugula neritina and the barnacle Balanus amphitrite, are major marine fouling ...
Yi-Fan Zhang   +4 more
doaj   +1 more source

Synthesis, Characterization and Chemistry of Tetrakis(Propargylisocyanide) Copper(I) Complex

open access: yesMolbank, 2023
The kinetically unstable propargylisocyanide was reacted with the tetrakis(acetonitrile) copper(I) hexafluorophosphate and the formed complex was then involved in a copper-catalyzed alkyne-azide cycloaddition reaction (CuAAC). After the decomplexation of
Alexandre Quelhas   +3 more
doaj   +1 more source

The isocyanide SN2 reaction

open access: yesNature Communications, 2023
Abstract The S N 2 nucleophilic substitution reaction is a vital organic transformation used for drug and natural product synthesis. Nucleophiles like cyanide, oxygen, nitrogen, sulfur, or phosphorous replace halogens or sulfonyl esters, forming new bonds.
Patil, Pravin   +3 more
openaire   +4 more sources

Synthesis and Biological Activities of Luminescent 5,6-Membered Bis(Metallacyclic) Platinum(II) Complexes

open access: yesMolecules, 2023
Four couples of 5,6-membered bis(metallacyclic) Pt(II) complexes with acetylide and isocyanide auxiliary ligands have been prepared and characterized.
Jing Jing   +7 more
doaj   +1 more source

Isocyanides: Promising Functionalities in Bioorthogonal Labeling of Biomolecules

open access: yesFrontiers in Chemistry, 2021
Isocyanides have drawn increasing attention in biological applications due to their attractive properties and unique reactivities, which can undergo various reactions, such as multicomponent reactions, α-addition reactions, [4 + 1] cycloaddition ...
Yuchen Zhu   +6 more
doaj   +1 more source

Divergent isoindolinone synthesis through palladium-catalyzed isocyanide bridging C–H activation

open access: yesCell Reports Physical Science, 2022
Summary: The formation of thermodynamically accessible metallacycle is crucial to achieve site-selective C–H bond activation. Here, we report an isocyanide-bridging C–H activation through the formation of a five-membered palladacycle. As such, a proximal
Fulin Zhang   +6 more
doaj   +1 more source

From sequence-defined macromolecules to macromolecular pin codes [PDF]

open access: yes, 2020
Dynamic sequence-defined oligomers carrying a chemically written pin code are obtained through a strategy combining multicomponent reactions with the thermoreversible addition of 1,2,4-triazoline-3,5-diones (TADs) to indole substrates.
Badi, Nezha   +4 more
core   +1 more source

Potential Original Drug for Aspergillosis: In Vitro and In Vivo Effects of 1-N,N-Dimethylamino-5-Isocyanonaphthalene (DIMICAN) on Aspergillus fumigatus

open access: yesJournal of Fungi, 2022
As the recent outbreak of coronavirus disease 2019 (COVID-19) has shown, viral infections are prone to secondary complications like invasive aspergillosis with a high mortality rate, and therefore the development of novel, effective antifungals is of ...
Zsuzsa Máthéné Szigeti   +8 more
doaj   +1 more source

Homocoupling of CO and isocyanide mediated by a C,C′-bis(silylenyl)-substituted ortho-carborane [PDF]

open access: yes, 2019
The unexpected reactivity of the o-carborane supported bis-silylene [(LSi:)C]2B10H101 {L= PhC(tBuN)2} towards carbon monoxide and 2,6-dimethylphenyl isocyanide is reported.
Drieß, Matthias   +4 more
core   +1 more source

Conductance of a single molecule anchored by an isocyanide substituent to gold electrodes [PDF]

open access: yes, 2006
The effect of anchoring group on the electrical conductance of a single molecule bridging two Au electrodes was studied using di-substituted (isocyanide (CN-), thiol (S-) or cyanide (NC-)) benzene.
Cunningham I. D.   +5 more
core   +2 more sources

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