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 …

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 …

Abstract The palladium‐catalyzed Suzuki–Miyaura reaction of multiply halogenated,
electron‐rich and electron‐deficient heteroarenes is one of the most reliable and …

A modular synthesis of the lamellarin family of natural products has been developed that is
based on the application of three iterative halogenation/cross-coupling reaction sequences …

The HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs) constitute a large and
structurally diverse set of compounds, several of which are currently used in the treatment of …

The synthetic chemistry of the pyrrolic unit is dominated by electrophilic aromatic substitution
and pyrrole is much more reactive than benzene in this respect, as a result of the lone pair at …

Attenuation of protein kinases by selective inhibitors is an extremely active field of activity in
anticancer drug development. Therefore, Akt, a serine/threonine protein kinase, also known …

Palladium‐catalysed cross‐coupling reactions are routinely used in the synthesis of
important organic and organometallic compounds, including advanced materials and …

A practical and high-yielding protocol for the dehalogenation of aromatic halides is
presented. In the presence of palladium acetate, triphenylphosphine, and potassium …

The efficient Suzuki–Miyaura cross-coupling reaction of halogenated aminopyrazoles and
their amides or ureas with a range of aryl, heteroaryl, and styryl boronic acids or esters has …