New enantiomerically pure 1,3-bis(2'-oxazolinyl)ferrocenes have been synthesized in good yields starting from 1,3-ferrocene dicarboxylic acid. Moreover, the possibility of performing a regioselective lithiation in position 2 of the disubstituted cyclopentadienyl ring of these compounds has been demonstrated.
Bonini B., Capitò E., Comes-Franchini M., Fochi M., Ricci A. (2006). Synthesis of new enantiomerically pure 1,3-bis-(2’-oxazolinyl)ferrocenes as potential pincer ligands. ARKIVOC, VI, 85-96.
Synthesis of new enantiomerically pure 1,3-bis-(2’-oxazolinyl)ferrocenes as potential pincer ligands
BONINI, BIANCA FLAVIA;CAPITO', ELENA;COMES FRANCHINI, MAURO;FOCHI, MARIAFRANCESCA;RICCI, ALFREDO MARCO
2006
Abstract
New enantiomerically pure 1,3-bis(2'-oxazolinyl)ferrocenes have been synthesized in good yields starting from 1,3-ferrocene dicarboxylic acid. Moreover, the possibility of performing a regioselective lithiation in position 2 of the disubstituted cyclopentadienyl ring of these compounds has been demonstrated.File in questo prodotto:
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