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.
Synthesis of new enantiomerically pure 1,3-bis-(2’-oxazolinyl)ferrocenes as potential pincer ligands / Bonini B.; Capitò E.; Comes-Franchini M.; Fochi M.; Ricci A.. - In: ARKIVOC. - ISSN 1551-7004. - STAMPA. - VI:(2006), pp. 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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