Abstract
Abstract Ter-pyridine derivatives were found to be potential catalyst for homoallylation of carbonyl groups. High yields of the products with short reaction times of ∼2 h were observed in several cases. These new catalysts work efficiently with the simple reagent such as allyl magnesium bromide and hence can avoid the use of other sensitive or toxic reagents. It was found that the presence of polar groups on the catalysts made them extremely efficient without the presence of any metal salts.
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