Chiral Phosphoric-Acid-Catalyzed Transfer Hydrogenation of Ethyl Ketimine Derivatives by Using Benzothiazoline

被引:31
|
作者
Saito, Kodai [1 ]
Horiguchi, Kosaku [1 ]
Shibata, Yukihiro [2 ,3 ]
Yamanaka, Masahiro [2 ,3 ]
Akiyama, Takahiko [1 ]
机构
[1] Gakushuin Univ, Fac Sci, Dept Chem, Toshima Ku, Tokyo 1718588, Japan
[2] Rikkyo Univ, Fac Sci, Dept Chem, Toshima Ku, Tokyo 1718501, Japan
[3] Rikkyo Univ, Fac Sci, Res Ctr Smart Mol, Toshima Ku, Tokyo 1718501, Japan
关键词
hydrogen donor; hydrogenation; organocatalysis; reductive amination; theoretical studies; ASYMMETRIC TRANSFER HYDROGENATION; ORGANOCATALYTIC REDUCTIVE AMINATION; HIGHLY ENANTIOSELECTIVE REDUCTION; FRIEDEL-CRAFTS REACTIONS; MANNICH-TYPE REACTION; BRIDGED NADH MODELS; BRONSTED ACID; TRANSITION-METAL; HANTZSCH ESTERS; ALPHA; BETA-UNSATURATED ALDEHYDES;
D O I
10.1002/chem.201402763
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chiral phosphoric acid catalyzed transfer hydrogenation of ketimines derived from propiophenone derivatives and reductive amination of alkyl ethyl ketone derivatives were extensively examined in the presence of two representative hydrogen donors. The excellent enantioselective transfer hydrogenation was achieved by use of benzothiazoline as a hydrogen donor. The theoretical studies elucidated that the unsymmetrical structure of benzothiazoline plays an important role in high enantioselective hydrogenation.
引用
收藏
页码:7616 / 7620
页数:5
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