One-Pot Tandem Approach to Functionalized 3-Hydroxy-2-furanyl-acrylamides

被引:5
|
作者
Mupparapu, Nagaraju [1 ]
Khan, Shahnawaz [1 ,2 ]
Bandhoria, Pankaj [3 ]
Athimoolam, Shunmuganarayanan [4 ]
Ahmed, Qazi Naveed [1 ,2 ]
机构
[1] IIIM, Med Chem Div, Jammu 180001, India
[2] Acad Sci & Innovat Res AcSIR IIIM, Jammu 180001, India
[3] GGM Sci Coll, Dept Phys, Jammu 180001, India
[4] Anna Univ Technol Tirunelveli, Univ Coll Engn Nagercoil, Dept Phys, Nagercoil 629004, India
来源
ACS OMEGA | 2018年 / 3卷 / 05期
关键词
POLYSUBSTITUTED FURANS; ORGANIC-SYNTHESIS; FACILE SYNTHESIS; 2,5-DISUBSTITUTED FURANS; TETRASUBSTITUTED FURANS; H FUNCTIONALIZATION; SUBSTITUTED FURANS; ATOM ECONOMY; DERIVATIVES; CYCLIZATION;
D O I
10.1021/acsomega.8b00715
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel one-pot tandem process involving Knoevenagel condensation, Michael addition, selective amidation, and Paal-Knorr cyclization to diverse functionalized 3-hydroxy-2-furanyl-acrylamides from simple 2-oxoaldehydes and aroylacetonitriles was presented. Attempts were also made to expand the scope of the reaction to different 2-heteroarylfurans. The packing diagram of the molecules viewed down along the a-axis of the unit cell showed a characteristic intramolecular classical O-H center dot center dot center dot O hydrogen bond between hydroxyl and carbonyl O atoms leading to self-associated (Z)-2-furanyl-acrylamides.
引用
收藏
页码:5445 / 5452
页数:8
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