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MacMillan催化剂水相不对称催化Aldol反应

MacMillan Catalyst for the Asymmetric Aldol Reactions in Water
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摘要 以自制的手性MacMillan催化剂MM3-2与1当量HCl,在水相中不对称催化环酮与芳香醛的反应,以中等的产率、较高的dr值与ee值得到Aldol反应产物,实现了MacMillan催化剂在水相中对Aldol反应的催化。 A chiral MacMillan catalyst was synthesized and used with acid in the direct Aldol reactions in water as organocatalyst. Using the catalyst the aldol product was obtained in much higher dr values, ee values and yield in comparison to that was observed using other ganocatalysts.
作者 黄勤安
出处 《黄山学院学报》 2008年第5期41-43,共3页 Journal of Huangshan University
关键词 MacMillan催化剂 不对称催化 ALDOL反应 MacMillan catalyst asymmetric catalyst Aldol reaction
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参考文献3

  • 1D.A.Evens,D.M.Fitch,T.E.Smith,V.J.Cee.Application of Complex Aldol Reactions to the Total Synthesis ofPhorboxazole B[].Journal of the American Chemical Society.2000
  • 2N.Mase,Y.Nakai,N.Ohara,H.Yoda,K.Takabe,F.Tanaka,C.F.Barbas.Organocatalytic Direct Asymmetric AldolReactions in Water[].Journal of the American Chemical Society.2006
  • 3Austin J. F.,MacMillan D. W. C.Enantioselective organocatalytic indole alkylations. Design of a new and highly effective chiral amine for iminium catalysis[].Journal of the American Chemical Society.2002

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