作者:Teruaki Mukaiyama、Nobuharu Iwasawa、Rodney W. Stevens、Toru Haga
DOI:10.1016/s0040-4020(01)82423-6
日期:1984.1
A highly diastereoselective cross aldolreaction is developed using divalent tin enolates formed from stannous trifluoromethanesulfonate and carbonyl compounds. The reaction is extended to a highly enantioselective cross aldolreaction employing chiral diamines derivedfrom (S)-proline as ligands.
Cerium enolates formed from cerium (III) chloride and lithium enolates undergo aldolreaction with ketones or sterically crowded aldehydes to afford the corresponding β-hydroxyketones in high yields.