In industries and academic laboratories, several late transition metal-catalyzed prerequisite
reactions are widely performed during single and multistep synthesis. However, besides the …

The present review “Iron Catalysis in Organic Synthesis” covers the literature until the end of
June 2014 and represents a comprehensive update of a previous article published by Bolm …

The development of efficient Friedel–Crafts alkylations of arenes and heteroarenes using
only catalytic amounts of a Lewis acid has gained much attention over the last decade. The …

A simple, convenient, and multicomponent coupling strategy for the synthesis of highly
functionalized pyrroles catalyzed by iron (III) salts has been developed. This strategy …

Abstract In 2005, the ACS Green Chemistry Institute (GCI) and the global pharmaceutical
corporations developed the ACS GCI Pharmaceutical Roundtable to encourage the …

Oxygen‐based electrophiles have emerged as some of the most valuable cross‐coupling
partners in organic synthesis due to several major strategic and environmental benefits …

New pyrazole and pyrazoline derivatives have been synthesized and their ability to inhibit
ovine COX-1/COX-2 isozymes was evaluated using in vitro cyclooxygenase (COX) inhibition …

Alcohols are abundant and attractive feedstock molecules for organic synthesis. Many
methods for their functionalization require them to first be converted into a more activated …

Direct nucleophilic substitution reactions of allylic alcohols are environmentally friendly,
since they generate only water as a byproduct, allowing access to new allylic compounds …

The eco-friendly and highly diastereoselective synthesis of substituted cis-2, 6-piperidines
and cis-2, 6-tetrahydropyrans is described. The key step of this method is the iron-catalyzed …