- an
alkyne to form a 5-membered
heteroatom ring: a
Cu(I)-catalyzed azide-alkyne
cycloaddition (
CuAAC). The
first triazole synthesis, from
diethyl acetylenedicarboxylate...
-
supported during the
process of copper(I)-catalyzed azide-alkyne
cycloaddition (
CuAAC). Goreshnik,
Evgeny (12 June 2021). "Copper(I)
azide and copper(I) cyanate...
- azide-alkyne
cycloaddition (Ru
AAC)
gives the 1,5-triazole.
Unlike CuAAC in
which only
terminal alkynes reacted, in Ru
AAC both
terminal and
internal alkynes...
- in
click chemistry. It is well
known that
intracellular Cu(I) is cytotoxic,
which means CuAAC is not as
common as
SPAAC click reactions for
research leading...
-
allowing for the
catalytic cycle of the
CuAAC reaction to proceed.
Single crystal X-ray
diffraction of the
Cu(I)
complex of tris((1-benzyl-4-triazolyl)methyl)amine...
- Cisnetti, Federico; Gautier,
Arnaud (2014). "[{
Cu(IPr)}2(μ-OH)][BF4]:
Synthesis and Halide-Free
CuAAC Catalysis".
Chemical Communications. 50 (54): 7154–7156...
-
click chemistry through copper(I)-catalyzed azide-alkyne
cycloaddition (
CuAAC) reactions,
where copper(I)
catalyzes the
cycloaddition of an organoazide...
- azide-alkyne
cycloaddition (
CuAAC), copper(I)
salts select for the
formation of 1,4-disubstituted 1,2,3-triazoles. One such
catalyst is
CuBr(PPh3)3,
which is relatively...
-
Copenhagen in Copenhagen, Denmark. He is best
known for
developing the
CuAAC-click reaction,
concurrently with but
independent of
Valery V.
Fokin and...
- cell imaging.
Although the mild, copper-catalyzed
variant of the reaction,
CuAAC (copper-catalyzed azide–alkyne cycloaddition) with
linear alkynes had been...