Results 151 to 160 of about 9,957 (210)

Supramolecular assembly properties of a mixed-sequence recognition-encoded melamine oligomer.

Org Biomol Chem
Dhiman M, Smith JT, Hunter CA.
europepmc   +1 more source

The Development of Antibody-Functionalized Liposomes via Click Chemistry for Precision Targeting of PD-L1-Positive Ovarian Cancer. [PDF]

ACS Omega
Chatterjee BP, Ghosh M, Dasgupta U, Chatterjee I, Agrawal S, Singh S, Chowdhury AD, Das P.   +7 more
europepmc   +1 more source

Late-stage peptide modification with salicylaldehyde tag enhances affinity for nuclear factor-kappa B essential modulator. [PDF]

RSC Chem Biol
Mason M, Peqini K, Uggeri F, Rondelli D, Sattin S, Pignataro L, Pellegrino S, Belvisi L, Scarpa E, Bucci R, Dal Corso A.   +10 more
europepmc   +1 more source

Engineering protein prenylation: an emerging tool for selective protein modification. [PDF]

Biochem Soc Trans
Venkatachalapathy S, Lichtenfels C, Wagner CR, Distefano MD.   +3 more
europepmc   +1 more source

From Molecule to Meaning: Click and Bioorthogonal Chemical Reporters for Plant Systems, Biological Imaging, and Artistic Expression. [PDF]

Chembiochem
Hinnebo M, Simon C, Tilouine A, Spriet C, Biot C.   +4 more
europepmc   +1 more source

Rational design of click-assembled chiral dendrimers: anticancer activity and molecular dynamics study. [PDF]

RSC Adv
El Malah T, El-Rashedy AA.
europepmc   +1 more source

Borane-functionalized heteroscorpionate copper complexes as catalysts for azide-alkyne cycloaddition.

Dalton Trans
Cruz TFC, López-Sánchez B, Lemos MANDA, Romerosa A, Martins LMDRS.   +4 more
europepmc   +1 more source

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Arylazopyrazoles for Conjugation by CuAAC Click Chemistry

The Journal of Organic Chemistry
Molecular photoswitches are increasingly being implemented in bioactive compounds and responsive materials. For this purpose, photoswitches must be coupled to a wide variety of substrates and scaffolds. We present a library of "clickable" arylazopyrazoles (AAPs), which can be conjugated by Cu-catalyzed alkyne azide cycloaddition (CuAAC).
Alisa-Maite Kauth, Rebecca Niebuhr, Bart Jan Ravoo   +2 more
openaire   +3 more sources

Recent Fascinating Aspects of the CuAAC Click Reaction

Trends in Chemistry, 2020
CuAAC chemistry is used to compose incredible synthetic molecular architectures and acts as a true click chemistry reaction allowing densely functional molecular fragments to be joined in a highly controlled manner. Using supercatalysts based on our mechanistic understanding and in the absence of oxygen, CuAAC reactions are superior even in bioligation
Meldal, Morten, Diness, Frederik
openaire   +3 more sources

CuAAC-Based Click Chemistry in Self-Healing Polymers

Accounts of Chemical Research, 2017
Click chemistry has emerged as a significant tool for materials science, organic chemistry, and bioscience. Based on the initial concept of Barry Sharpless in 2001, the copper(I)-catalyzed azide/alkyne cycloaddition (CuAAC) reaction has triggered a plethora of chemical concepts for linking molecules and building blocks under ambient conditions, forming
Diana Döhler, Philipp Michael, Wolfgang H. Binder   +2 more
openaire   +3 more sources