Chem. J. Chinese Universities ›› 2004, Vol. 25 ›› Issue (4): 651.

• Articles • Previous Articles     Next Articles

Asymmetric Aminohydroxylation of Olefins Catalyzed by 1,4-Bis(9-O-quininyl)phthalazine-OsO4 Complex

CHENG Si-Kun, KUANG Yong-Qing, LU Li-Hua, LI Xiao-Ye, ZHANG Sheng-Yong   

  1. Teaching and Research Section of Chemistry, the 4th Military Medical University, Xi′an 710032, China
  • Received:2003-03-24 Online:2004-04-24 Published:2004-04-24

Abstract: Five olefins were aminohydroxylated enantiomerically catalyzed by 1,4-bis(9-O-quininyl)phthalazine-OsO4 complex in the presence of benzyl N-chlorocarbamate(oxidant and nitrogen source). Excellent enantioselectivity(85%—99% e.e.) as well as specific regio and chemoselectivity were observed and isolated yield of the products 48%—68% was achieved. The results are comparable to those of the best catalyst reported for AA reaction.

Key words: Bis(9-O-quininyl)phthalazine, Asymmetric aminohydroxylation, Chiral β-amino alcohol

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