Copper-Catalyzed C–H Functionalization Reactions: Efficient Synthesis of Heterocycles |
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The copper‐catalyzed alkyne‐azide cycloaddition (CuAAC) is a highly versatile,
regioselective synthesis of 1, 4‐disubstituted 1, 2, 3‐triazoles under mild reaction conditions …

An efficient copper-catalyzed synthesis of 1, 2, 4-trisubstituted imidazoles using amidines
and terminal alkynes has been developed. Overall, the oxidative process, which involves …

Here a new, mild and versatile method for one-pot cascade synthesis of diverse N-
methoxyisoquinolinediones via Rh (III)-catalyzed regioselective carbenoid insertion C–H …

The past decade has seen the development of a new reactivity concept, exploiting the
ubiquity of C–H bonds. The direct activation of this bond type brings forth a straightforward …

Mono-N-arylation of benzamidines 1 with aryl boronic acids 2 was effectively achieved in the
presence of a catalytic amount of Cu (OAc) 2 and NaOPiv under mild aerobic conditions …

Ligand-free hydroboration of alkynes catalyzed by heterogeneous copper powder with high
efficiency - Chemical Communications (RSC Publishing) DOI:10.1039/C3CC48670B Royal …

Indoles are important structural motifs that are commonly found in a diverse array of natural
products, pharmaceuticals, and other functional molecules. Consequently, the development …

Ruthenium-Catalyzed Cycloisomerization of 2-Alkynylanilides: Synthesis of 3-Substituted
Indoles by 1,2-Carbon Migration | Journal of the American Chemical Society ACS ACS …

Oxadiazoles experienced an almost 80-year long period of scientific lethargy before they
tickled the curiosity of chemists. The study of chemical and photochemical reactivity of 1, 2, 4 …