Copper-Catalyzed C–H Functionalization Reactions: Efficient Synthesis of Heterocycles |
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Covering: 2013. Previous review: Nat. Prod. Rep., 2014, 31, 160–258 This review covers the
literature published in 2013 for marine natural products (MNPs), with 982 citations (644 for …

The ynamide functional group activates carbon–carbontriple bonds through an attached
nitrogen atom that bears an electron-withdrawing group. As a result, the alkyne has both …

Ynamides are special alkynes bearing an electron-withdrawing group on the nitrogen atom,
and they have been extensively studied over the past decade. However, the addition of …

Conspectus Vicinal diamines are important structural motifs present in various biologically
and chemically significant molecules. Direct diamination of olefins provides an effective …

The synthesis of N-heterocycles is one of the most active areas due to their structures with
extensive applications in the fields of organic, pharmaceutical and materials chemistry. It is …

Development of C–N coupling processes is fundamentally important and challenging for the
synthesis of biologically active molecules and drugs. Herein, we report a highly atom …

We have developed a visible light-induced photo-redox copper-catalyzed oxidative Csp2–H
annulation (Friedel–Crafts-type cyclization) of amidines with terminal alkynes at room …

Nitrogen‐containing heterocycles have found remarkable applications in natural product
research, material sciences, and pharmaceuticals. Although the synthesis of this interesting …

Selective cleavage of C–C bonds forms one of the greatest challenges in current organic
chemistry, due to the relative strength of these bonds. However, such transformations are an …