Two new diastereomeric ferrocenyl triphosphine ligands P3Chir 1 and 2 have been conveniently synthesized through a multistep reaction sequence starting from (R)-(S)-diphenylphosphinoferrocenylamine [(R)-(S)-PPFA]. Chromatographic resolution of the diborane protected-phosphine oxide derivatives, followed by a stereoconservative reduction/deboronation step, gave the pure triphosphines P3Chir in which the planar chirality of the ferrocenyl unit is combined with phosphorus and carbon stereocenters in an unprecedented molecular assembly.

Synthetic Approaches to New Diastereomerically Pure Ferrocenyl Triphosphines Combining Phosphorous, Planar and Carbon Chirality / Barbaro P; Bianchini C; Giambastiani G; Masi D; Parisel S L; Togni A. - In: SYNTHESIS. - ISSN 0039-7881. - STAMPA. - (2004), pp. 345-352. [10.1055/s-2003-44378]

Synthetic Approaches to New Diastereomerically Pure Ferrocenyl Triphosphines Combining Phosphorous, Planar and Carbon Chirality

Giambastiani G;
2004

Abstract

Two new diastereomeric ferrocenyl triphosphine ligands P3Chir 1 and 2 have been conveniently synthesized through a multistep reaction sequence starting from (R)-(S)-diphenylphosphinoferrocenylamine [(R)-(S)-PPFA]. Chromatographic resolution of the diborane protected-phosphine oxide derivatives, followed by a stereoconservative reduction/deboronation step, gave the pure triphosphines P3Chir in which the planar chirality of the ferrocenyl unit is combined with phosphorus and carbon stereocenters in an unprecedented molecular assembly.
2004
345
352
Barbaro P; Bianchini C; Giambastiani G; Masi D; Parisel S L; Togni A
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1352157
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