Pyrrolidine catalyzed regioselective and diastereoselective direct aldol reaction in water
Dinesh Mahajan, Swapandeep Singh Chimni
Abstract
Dinesh Mahajan, Swapandeep Singh Chimni
Abstract
Pyrrolidine catalyzed direct aldol reaction of methyl ketones other than acetone with 4-nitrobenzaldehyde in water affords linear aldol addition product arising from the selective attack of the unsubstituted carbon of the unsymmetrical ketone. The present methodology provides an experimentally simple and green process for regioselective synthesis of β-hydroxyketones in water.
OpenAlex reports 3 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Pyrrolidine catalyzed direct aldol reaction of methyl ketones other than acetone with 4-nitrobenzaldehyde in water affords linear aldol addition product arising from the selective attack of the unsubstituted carbon of the unsymmetrical ketone. The present methodology provides an experimentally simple and green process for regioselective synthesis of β-hydroxyketones in water.
Key concepts: Aldol reaction, Regioselectivity, Pyrrolidine, Ketone, Chemistry, Acetone, Catalysis, Aldol condensation