The design of synthetic routes by retrosynthetic logic is decisively influenced by the
transformations available. Transition‐metal‐catalyzed C− H activation has emerged as a …

Methods to functionalize arenes and heteroarenes in a site-selective manner are highly
sought after for rapidly constructing value-added molecules of medicinal, agrochemical, and …

Marine organisms have proven to be rich sources of unique alkaloids. In earlier surveys we
comprehensively reviewed several intriguing groups of marine alkaloids, including the …

A general method is presented for the synthesis of alkylated arenes by the chemoselective
combination of two electrophilic carbons. Under the optimized conditions, a variety of aryl …

Five-membered heterocycle derivatives with two aryl groups on adjacent positions include
several classes of natural and unnatural compounds that exhibit a variety of biological and …

Synthesis of natural products containing the pyrrolic ring - Natural Product Reports (RSC
Publishing) DOI:10.1039/C0NP00014K Royal Society of Chemistry View PDF VersionPrevious …

This tutorial review focuses on several practical synthetic transformations utilising palladium
catalysis that facilitate the synthesis of functionalised unsaturated heterocycles in a …

A new catalyst system for the Pd-catalyzed cross-coupling of organozinc reagents with aryl
halides (Negishi coupling) has been developed. This system permits efficient preparation of …

Lamellarins are natural products isolated from marine invertebrates having a unique
heterocyclic ring system. Many of these natural products exhibit potentially useful biological …

Lamellarins are marine alkaloids containing fused 14-phenyl-6H-[1] benzopyrano [4′, 3′:
4, 5] pyrrolo [2, 1-a] isoquinoline or non-fused 3, 4-diarylpyrrole-2-carboxylate ring systems …