Molecular iodine-catalyzed multicomponent reactions: an efficient catalyst for organic synthesis

被引：201

作者：

Ren, Yi-Ming ^{[1
]}

Cai, Chun ^{[2
]}

Yang, Ren-Chun ^{[1
]}

机构：

[1] Anhui Polytech Univ, Dept Biochem Engn, Wuhu 241000, Peoples R China

[2] Nanjing Univ Sci & Technol, Chem Engn Coll, Nanjing 210094, Jiangsu, Peoples R China

来源：

RSC ADVANCES | 2013年 / 3卷 / 20期

基金：

中国国家自然科学基金;

关键词：

ONE-POT SYNTHESIS; HIGHLY SELECTIVE METHOD; SOLVENT-FREE CONDITIONS; DIELS-ALDER REACTIONS; ELECTRON-RICH ARENES; BETA-AMINO KETONES; FACILE SYNTHESIS; CARBONYL-COMPOUNDS; VERSATILE CATALYST; DOMINO REACTION;

D O I：

10.1039/c3ra23461d

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The multicomponent reactions (MCRs) consist of two or more synthetic steps which are carried out without isolation of any intermediate thus reducing time, saving money, energy and raw materials. The development of MCRs in the presence of molecular iodine is an efficient approach that meets with the requirements of sustainable chemistry. The aim of this review is to highlight the synergistic effect of the combined use of MCRs and molecular iodine for the development of new eco-compatible methodologies for organic chemistry.

引用

页码：7182 / 7204

页数：23

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