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 …

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

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 …

FeCl3-catalyzed Ritter reaction. Synthesis of amides - ScienceDirect Skip to main contentSkip
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A new protocol for the direct sulfonylation of benzylic, allylic and homoallylic alcohols with
sodium arenesulfinates is described by using iron (III) chloride as a catalyst and …

The review describes the state of the art in hydration reactions of alkynes by direct or indirect
catalysis of first row transition metal complexes, covering mostly the literature of the last …

An efficient Fe (III)-catalyzed direct coupling of alkenes with alcohols and cross-coupling of
alcohols with alcohols to give the corresponding substituted (E)-alkenes stereospecifically is …

Iron catalysts are extensively used in organic reactions in recent years since iron is one of
the most abundant metals on earth, consequently one of the most inexpensive, and …

Although they have been used as reactivity-controlling additives in cationic polymerizations
for decades, Lewis basic “electron pair donor”(ED) compounds were never used for the …