Functionalized chiral indole derivatives are privileged and versatile organic frameworks
encountered in numerous pharmaceutically active agents and biologically active natural …

Abstract β-Carboline alkaloids are a family of natural and synthetic products with great
structural diversity and outstanding biological activities. This review covers critically …

The extraordinary impact of metal-based complexes on synthetic methods is still recognized
nowadays, and attempts are currently undertaken to further extend the use of metal-assisted …

From tryptamine and secologanine, nature generates monoterpene indole alkaloids with an
unprecedented level of skeletal diversity through a 'couple–divert'sequence. Intrigued by this …

Vinylcyclopropanes (VCPs) are known to generate 1, 3-dipoles with a palladium catalyst that
initially serve as nucleophiles to undergo [3+ 2] cycloadditions with electron-deficient olefins …

Quinazolinones belong to a family of heterocyclic nitrogen compounds that have attracted
increasing interest because of their broad spectrum of biological functions. This review …

Here we report the oxidative umpolung of 2, 3-disubstituted indoles toward enantioselective
dearomative aza-spirocyclization to give the corresponding spiroindolenines using chiral …

The selective hydrogenation of benzofurans in the presence of a heterogeneous non‐noble
metal catalyst is reported. The developed optimal catalytic material consists of cobalt‐cobalt …

Indole alkaloids bearing the tetracyclic indoline scaffolds of 1H‐pyrrolo [2, 3‐d] carbazole
have shown fascinating chemical diversity and significant biological activities. The …

The pseudoindoxyl sub-structural motif, amongst the large set of the indole class of
alkaloids, represents a unique subset of the oxygenated indole class of the alkaloid family. A …