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.
引用
收藏
页码:6470 / 6473
页数:4
相关论文
共 88 条
[71]   Highly Efficient Small Organic Molecules for Enantioselective Direct Aldol Reaction in Organic and Aqueous Media [J].
Vishnumaya, Monika Raj ;
Singh, Vinod K. .
JOURNAL OF ORGANIC CHEMISTRY, 2009, 74 (11) :4289-4297
[72]   Highly Efficient Direct Asymmetric Aldol Reactions Catalyzed by a Prolinethioamide Derivative in Aqueous Media [J].
Wang, Bing ;
Liu, Xin-wang ;
Liu, Ling-yan ;
Chang, Wei-xing ;
Li, Jing .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2010, 2010 (31) :5951-5954
[73]   Direct, facile aldehyde and ketone α-selenenylation reactions promoted by L-prolinamide and pyrrolidine sulfonamide organocatalysts [J].
Wang, J ;
Li, H ;
Mei, YJ ;
Lou, BS ;
Xu, DG ;
Xie, DQ ;
Guo, H ;
Wang, W .
JOURNAL OF ORGANIC CHEMISTRY, 2005, 70 (14) :5678-5687
[74]   Proline-catalyzed asymmetric aldol reactions of tetrahydro-4H-thiopyran-4-one with aldehydes [J].
Ward, DE ;
Jheengut, V .
TETRAHEDRON LETTERS, 2004, 45 (45) :8347-8350
[75]   Simple and inexpensive threonine-based organocatalysts as highly active and recoverable catalysts for large-scale asymmetric direct stoichiometric aldol reactions on water [J].
Wu, Chuanlong ;
Long, Xiaoqin ;
Li, Shi ;
Fu, Xiangkai .
TETRAHEDRON-ASYMMETRY, 2012, 23 (05) :315-328
[76]   New simple and recyclable O-acylation serine derivatives as highly enantioselective catalysts for the large-scale asymmetric direct aldol reactions in the presence of water [J].
Wu, Chuanlong ;
Fu, Xiangkai ;
Li, Shi .
TETRAHEDRON, 2011, 67 (23) :4283-4290
[77]   Simple, inexpensive, and facile L-prolinamide used as a recyclable organocatalyst for highly efficient large-scale asymmetric direct aldol reactions [J].
Xu, Jiangwei ;
Fu, Xiangkai ;
Wu, Chuanlong ;
Hu, Xiaoyan .
TETRAHEDRON-ASYMMETRY, 2011, 22 (08) :840-850
[78]   Enamine-Metal Lewis Acid Bifunctional Catalysis: Application to Direct Asymmetric Aldol Reaction of Ketones [J].
Xu, Zhenghu ;
Daka, Philias ;
Budik, Ilya ;
Wang, Hong ;
Bai, Fu-Quan ;
Zhang, Hong-Xing .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2009, 2009 (27) :4581-4585
[79]   N-(p-Dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide: A Practical Proline Mimetic for Facilitatina Enantioselective Aldol Reactions [J].
Yang, Hua ;
Carter, Rich G. .
ORGANIC LETTERS, 2008, 10 (20) :4649-4652
[80]   Highly Stereoselective and Scalable anti-Aldol Reactions Using N-(p-Dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide: Scope and Origins of Stereoselectivities [J].
Yang, Hua ;
Mahapatra, Subham ;
Cheong, Paul Ha-Yeon ;
Carter, Rich G. .
JOURNAL OF ORGANIC CHEMISTRY, 2010, 75 (21) :7279-7290