Results 11 to 20 of about 2,940,757 (378)

Orthogonal, metal-free surface modification by strain-promoted azide–alkyne and nitrile oxide–alkene/alkyne cycloadditions [PDF]

open access: yes, 2012
In this article we present a fast and efficient methodology for biochemical surface patterning under extremely mild conditions. Micropatterned azide/benzaldoxime-surfaces were prepared by microcontact printing of a heterobifunctional cyclooctyne oxime ...
Arlinghaus, Heinrich F   +6 more
core   +2 more sources

The effect of zinc oxide nanoparticle morphology on activity in crosslinking of carboxylated nitrile elastomer

open access: diamondeXPRESS Polymer Letters, 2009
The aim of this work was to study the activity of several nanosized zinc oxides in the crosslinking of carboxylated nitrile elastomer (XNBR). In this article, we discuss the effect of zinc oxide nanoparticles with respect to their specific surface area ...
M. Przybyszewska, Marian Zaborski
doaj   +2 more sources

Selective covalent targeting of GPX4 using masked nitrile-oxide electrophiles. [PDF]

open access: yesNat Chem Biol, 2020
Eaton JK   +22 more
europepmc   +2 more sources

Rapid Metal -free Macromolecular Coupling via in situ Nitrile Oxide-Activated Alkene Cycloaddition. [PDF]

open access: yesJ Polym Sci A Polym Chem, 2014
Nitrile oxide 1,3 dipolar cycloaddition is a simple and powerful coupling methodology. However, the self-dimerization of nitrile oxides has prevented the widespread use of this strategy for macromolecular coupling.
Isaacman MJ, Cui W, Theogarajan LS.
europepmc   +2 more sources

An anomalous hydration/dehydration sequence for the mild generation of a nitrile oxide [PDF]

open access: yesOrganic and biomolecular chemistry, 2011
A nitrile oxide containing a carbamoyl group is readily generated upon the treatment of 2-methyl-4-nitro-3-isoxazolin-5(2H)-one with water under mild reaction conditions, even in the absence of special reagents.
884   +19 more
core   +3 more sources

Synthesis of Bicyclic Isoxazoles and Isoxazolines via Intramolecular Nitrile Oxide Cycloaddition [PDF]

open access: yesMolecules, 2015
An efficient and straight forward procedure for the syntheses of bicyclic isoxazole/isoxazoline derivatives from the corresponding dimethyl-2-(2-nitro-1-aryl/alkyl)-2-(prop-2-yn-1yl)malonates or dimethyl 2-allyl-2-(2-nitro-1-aryl/alkyl ethyl)malonate is ...
Wen-Chang Chen   +8 more
doaj   +2 more sources

Nitrile Oxide/Alkyne Cycloadditions – A Credible Platform for Synthesis of Bioinspired Molecules by Metal‐Free Molecular Clicking [PDF]

open access: bronze, 2012
The need for precise and flexible synthetic methodology to underpin modern research in chemical biology and materials science has fuelled a resurgence of interest in Huisgen 1,3-dipolar cycloaddition chemistry.
F. Heaney
semanticscholar   +2 more sources

Design and synthesis of amidine-type peptide bond isosteres: application of nitrile oxide derivatives as active ester equivalents in peptide and peptidomimetics synthesis. [PDF]

open access: yesOrganic and biomolecular chemistry, 2011
Amidine-type peptide bond isosteres were designed based on the substitution of the peptide bond carbonyl (C=O) group with an imino (C=NH) group. The positively-charged property of the isosteric part resembles a reduced amide-type peptidomimetic.
Fujii, Nobutaka   +7 more
core   +2 more sources

Synthesis of a Novel Tetracyclic Isoxazole by Intramolecular Nitrile Oxide Cycloaddition [PDF]

open access: goldMolbank
Intramolecular cycloadditions have the great advantage of forming two rings simultaneously. We report the use of intramolecular [3 + 2] cycloaddition of the nitrile oxide derived from an N-propargylbenzimidazole oxime in the synthesis of a hitherto ...
Gavin R. Hoffman, Allen M. Schoffstall
doaj   +2 more sources

Synthesis of β-D-ribofuranosylbenzazoles using nitrile oxide addition chemistry

open access: yesARKIVOC, 2012
A nitrile oxide based route to 2--D-ribofuranosylbenzazoles has been developed. Tri-Obenzoyl--D-ribofuranosylformonitrile oxide (14) was generated from the corresponding carbaldoxime 16 by treatment with NCS/pyridine, followed by base-induced ...
Iain A. S. Smellie, R. Michael Paton
doaj   +2 more sources

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