One-Pot Reactions: A Step Towards Greener Chemistry

被引：48
作者：
Sydnes, Magne O. [1 ]
机构：
[1] Univ Stavanger, Dept Math & Nat Sci, Fac Sci & Technol, NO-4036 Stavanger, Norway
来源：
CURRENT GREEN CHEMISTRY | 2014年 / 1卷 / 03期
基金：
日本学术振兴会;
关键词：
Cascade reactions; multicomponent reactions; one-pot reactions; stereospecific reactions; tandem synthesis;
D O I：
10.2174/2213346101666140221225404
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
One-pot reactions where several reaction sequences are conducted in the same reaction flask are one of the methods that can be used in order to conduct synthesis in a greener fashion. The chemistry is greener due to the reduction of work-up procedures and purification steps required compared to a more stepwise approach. In reactions that require a catalyst it is possible to combine several catalytic processes in the same reaction vessel. By highlighting a few of the recent success stories where multiple synthetic conversions are conducted in one reaction flask this minireview is aiming to show the power and benefits of one-pot multicomponent reactions.
引用
收藏
页码：216 / 226
页数：11
相关论文
共 114 条
[1]  
Ager DJ, 1997, ALDRICHIM ACTA, V30, P3
[2]  
[Anonymous], 1921, GAZZ CHIM ITAL
[3]   A one-pot synthesis of N-alkylaminobenzenes from nitroaromatics:: reduction followed by reductive amination using B10H14 [J].
Bae, JW ;
Cho, YJ ;
Lee, SH ;
Yoon, COM ;
Yoon, CM .
CHEMICAL COMMUNICATIONS, 2000, (19) :1857-1858
[4]   Asymmetric Mannich reactions catalyzed by cinchona alkaloid thiourea: enantioselective one-pot synthesis of novel β-amino ester derivatives [J].
Bai, Song ;
Liang, Xueping ;
Song, Baoan ;
Bhadury, Pinaki S. ;
Hu, Deyu ;
Yang, Song .
TETRAHEDRON-ASYMMETRY, 2011, 22 (05) :518-523
[5]   Pyrroles and gem-dihalocyclopropanes as building blocks for alkaloid synthesis [J].
Banwell, MG ;
Beck, DAS ;
Stanislawski, PC ;
Sydnes, MO ;
Taylor, RM .
CURRENT ORGANIC CHEMISTRY, 2005, 9 (15) :1589-1600
[6]   Synthesis of Pyrrole and Carbazole Alkaloids [J].
Bauer, Ingmar ;
Knoelker, Hans-Joachim .
ALKALOID SYNTHESIS, 2012, 309 :203-253
[7]   Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions [J].
Bellina, Fabio ;
Rossi, Renzo .
TETRAHEDRON, 2006, 62 (31) :7213-7256
[8]   Controlling the formation of 1 out of 64 stereoisomers using organocatalysis [J].
Bertelsen, Soren ;
Johansen, Rasmus L. ;
Jorgensen, Karl Anker .
CHEMICAL COMMUNICATIONS, 2008, (26) :3016-3018
[9]  
Biginelli P., 1891, BER DTSCH CHEM GES, V24, P2962, DOI DOI 10.1002/CBER.189102402126
[10]  
Biginelli P., 1891, BERICHTE DTSCH CHEM, V24, P1317, DOI DOI 10.1002/CBER.189102401228
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