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
Hauptverfasser: Ito, Masato, Osaku, Akihide, Kobayashi, Chika, Shiibashi, Akira, Ikariya, Takao
Format: Artikel
Sprache:eng
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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.
ISSN:0276-7333
1520-6041
DOI:10.1021/om801042b