潘圣强, 张从海, 严胜骄, 林军. 手性β-氨基醇催化的芳香醛对映选择性炔化反应[J]. 云南大学学报(自然科学版), 2011, 33(4): 445-448 .
引用本文: 潘圣强, 张从海, 严胜骄, 林军. 手性β-氨基醇催化的芳香醛对映选择性炔化反应[J]. 云南大学学报(自然科学版), 2011, 33(4): 445-448 .
PAN Sheng-qiang, ZHANG Cong-hai, YAN Sheng-jiao, LIN Jun. Chiral β-amino alcohol-catalyzed enantioselective alkynylationof Aromatic Aldehydes[J]. Journal of Yunnan University: Natural Sciences Edition, 2011, 33(4): 445-448 .
Citation: PAN Sheng-qiang, ZHANG Cong-hai, YAN Sheng-jiao, LIN Jun. Chiral β-amino alcohol-catalyzed enantioselective alkynylationof Aromatic Aldehydes[J]. Journal of Yunnan University: Natural Sciences Edition, 2011, 33(4): 445-448 .

手性β-氨基醇催化的芳香醛对映选择性炔化反应

Chiral β-amino alcohol-catalyzed enantioselective alkynylationof Aromatic Aldehydes

  • 摘要: 手性β-氨基醇是不对称催化反应中应用最为广泛的手性配体之一.以L-苯丙氨酸为原料简捷合成的手性β-氨基醇L*为手性配体,对不同取代芳香醛的对映选择性炔化反应进行了研究,结果表明其对该反应具有一定的不对称催化活性,光学收率(e.e值)最高达78.9%.

     

    Abstract: Chiral amino alcohols are one of the most widely employed types of ligands for asymmetric catalysis.In this paper,the easily prepared chiral tertiary amino alcohol L*,which was derived from L-phenylalanine,was found to catalyze the reaction of alkynylzinc reagents with various aldehydes to generate chiral propargylic alcohols with moderate-to-good enantioselectivities up to 78.9% e.e.

     

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