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Direct asymmetric aldol reaction co-catalyzed by L-proline and isothiouronium salts
被引:14
|作者:
Cho, Eun
[1
]
Kim, Taek Hyeon
[1
]
机构:
[1] Chonnam Natl Univ, Coll Engn, Sch Chem Engn, Kwangju 500757, South Korea
基金:
新加坡国家研究基金会;
关键词:
Aldol reaction;
Asymmetric catalysis;
Isothiouronium salt;
Solvent-free condition;
SOLVENT-FREE CONDITIONS;
BRONSTED ACID CATALYST;
METHYL KETONES;
EFFICIENT ORGANOCATALYSTS;
CONJUGATES SYNTHESIS;
L-PROLINETHIOAMIDES;
GOLD NANOPARTICLES;
PRIMARY AMINES;
WATER;
ALDEHYDES;
D O I:
10.1016/j.tetlet.2014.10.009
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
An efficient, simple, and highly selective protocol for the direct asymmetric aldol reaction between cyclohexanone and aromatic aldehydes using L-proline as a chiral catalyst is reported. Catalytic amounts of achiral isothiouronium iodide salt Id have been used for the first time as a co-catalyst for this reaction, which proved to be an excellent catalyst, producing good to excellent yields (up to 93%) with good stereoselectivities (up to 93:7 dr and 99% ee). These aldols are formed under solvent-free catalytic system, inside a standard laboratory refrigerator, and without stirring. (C) 2014 Elsevier Ltd. All rights reserved.
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页码:6470 / 6473
页数:4
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