Ammonium monovanadate (NH4VO3) has been devoted as an efficient, commercially available, eco-friendly and reusable catalyst for the synthesis of bis(indolyl)methanes (BIMs), oxindole derivatives and also Michael adducts of indoles at 50 °C under solvent-free conditions. The reusability of this solid acid catalyst in addition with its selectivity has also been examined.

Various isomers can be observed in the Friedel–Crafts alkylation of benzene. However, mechanism and influence these isomerization reactions were still unclear. In this work, several methyl phenylundecanoate analyzed by gas chromatography–mass spectrometry to explore alkylation. The results showed that there three reaction: five 6–10-phenylundecanoate due carbocation rearrangement, 6–9-methyldec...

The functionalisation of decalin by means of an "aliphatic Friedel-Crafts" reaction was reported over fifty years ago by Baddeley et al. This protocol is of current relevance in the context of C-H activation and here we demonstrate its applicability to a range of other saturated hydrocarbons. Structural elucidation of the products is described and a mechanistic rationale for their formation is ...

The Friedel-Crafts acylation is commonly used for the synthesis of aryl ketones, and a biocatalytic version, which may benefit from the chemo- and regioselectivity of enzymes, has not yet been introduced. Described here is a bacterial acyltransferase which can catalyze Friedel-Crafts C-acylation of phenolic substrates in buffer without the need of CoA-activated reagents. Conversions reach up to...

Over the last 8 years, our laboratory has developed the concept of iminium catalysis, a mode of LUMO-lowering activation that has enabled the invention of a large number of enantioselective organocatalytic transformations including Diels-Alder cycloadditions, Friedel-Crafts alkylations, Mukaiyama-Michael additions, hydrogenations, and heteroconjugate additions.1 Central to the utility of this t...