Gold(I)-Catalyzed Regioselective Hydroarylation of Propiolic Acid with Arylboronic Acids
Kolimi Sayyad Basha,
Rengarajan Balamurugan
Abstract:A gold-catalyzed intermolecular hydroarylation involving
arylboronic
acid has been disclosed. This carboxylic acid-directed arylation is
highly regioselective and occurs at the less electrophilic carbon
to afford α-aryl acrylic acids in attractive yields. This protocol
offers easy access to NSAID precursors.
“…74 Recently, Balamurugan and co-workers reported gold( i )-catalyzed Markovnikov-type selective hydroarylation of propiolic acid with organic boronic acids to α-carboxyl alkenes (Scheme 16(c)). 75…”
Metal-catalyzed highly Markovnikov-type selective hydrofunctionalization of terminal alkynes providing a straightforward and atom-economical route to access 1,1-disubstituted alkenes has been summarized.
“…74 Recently, Balamurugan and co-workers reported gold( i )-catalyzed Markovnikov-type selective hydroarylation of propiolic acid with organic boronic acids to α-carboxyl alkenes (Scheme 16(c)). 75…”
Metal-catalyzed highly Markovnikov-type selective hydrofunctionalization of terminal alkynes providing a straightforward and atom-economical route to access 1,1-disubstituted alkenes has been summarized.
A Pd-catalyzed regioselective hydroarylation/hydroalkenylation of terminal alkynes containing a heteroatom has been developed via carbopalladation for the synthesis of allylic ethers, amines, homoallylic alcohols and 1,3-dienes.
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