A Convenient Method for the Synthesis of Protic 2-(Tertiary phosphino)-1-amines and Their CpRuCl Complexes
A variety of protic 2-(tertiary phosphino)-1-amines (R2PCH2CHR′NHR′′, P−NH) have been prepared from 2-oxazolidinones and secondary phosphines using a newly developed acid-promoted decarboxylative C−P bond formation reaction. Treatment of the resulting chiral P−NH compounds with Cp*RuCl(isoprene) in...
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Veröffentlicht in: | Organometallics 2009-01, Vol.28 (2), p.390-393 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A variety of protic 2-(tertiary phosphino)-1-amines (R2PCH2CHR′NHR′′, P−NH) have been prepared from 2-oxazolidinones and secondary phosphines using a newly developed acid-promoted decarboxylative C−P bond formation reaction. Treatment of the resulting chiral P−NH compounds with Cp*RuCl(isoprene) in CH2Cl2 smoothly furnished chiral Cp*RuCl(P−NH) complexes with a typical three-legged piano-stool structure, which prove to be excellent catalyst precursors for asymmetric reactions, including the isomerization of allylic alcohols and hydrogenation of imides. |
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ISSN: | 0276-7333 1520-6041 |
DOI: | 10.1021/om801042b |