One-pot Multicomponent Synthesis of Highly Functionalized 1,4-Dihydropyridines Using Porcine Pancreatic Lipase

Ling Jiang , Wenting Ye , Weike Su

Chemical Research in Chinese Universities ›› 2019, Vol. 35 ›› Issue (2) : 235 -238.

PDF
Chemical Research in Chinese Universities ›› 2019, Vol. 35 ›› Issue (2) : 235 -238. DOI: 10.1007/s40242-019-8277-4
Article

One-pot Multicomponent Synthesis of Highly Functionalized 1,4-Dihydropyridines Using Porcine Pancreatic Lipase

Author information +
History +
PDF

Abstract

A series of highly functionalized 1,4-dihydropyridines was synthesized via one-pot multicomponent reactions of aromatic aldehyde, malononitrile and N-methyl-1-(methylthio)-2-nitroethenamine using Porcine pancreatic lipase(PPL) as catalyst in DMSO. This protocol is featured by mild reaction conditions, simple operation and environmental acceptability.

Keywords

Porcine pancreatic lipase / Biocatalysis / One-pot synthesis / Higly functionalized 1,4-dihydropyridines

Cite this article

Download citation ▾
Ling Jiang, Wenting Ye, Weike Su. One-pot Multicomponent Synthesis of Highly Functionalized 1,4-Dihydropyridines Using Porcine Pancreatic Lipase. Chemical Research in Chinese Universities, 2019, 35(2): 235-238 DOI:10.1007/s40242-019-8277-4

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Goto R. N., Sobral L. M., Sousa L. O., Garcia C. B., Lopes N. P., Marín-Prida J., Ochoa-Rodríguez E., Verdecia-Reyes Y., Pardo-Andreu G. L., Curti C., Leopoldino A. M. Eur. J. Pharmacol., 2018, 819: 198.

[2]

Desai N. C., Trivedi A. R., Somani H. C., Bhatt K. A. Chem. Biol. Drug Des., 2015, 86(3): 370.

[3]

Vijesh A. M., Isloor A. M., Peethambar S. K., Shivananda K. N., Arulmoli T., Isloor N. A. Eur. J. Med. Chem., 2011, 46(11): 5591.

[4]

Comins D. L., Smith E. D. Tetrahedron Lett., 2006, 47(9): 1449.

[5]

Isomura S., Horigome A., Kubo K., Yoshizawa Y., Okuno Y., Okayasu M., Azumaya I., Sato Y. Chemistry Select., 2018, 3(11): 3003.

[6]

Rao H. S. P., Parthiban A. Org. Biomol. Chem., 2014, 12(32): 6223.

[7]

Hajiyeva K., Ismiev A., Franz M., Schmidtmann M., Martens J., Maharramov A. Synth. Commun., 2017, 47(22): 2031.

[8]

Miao Y. F., Rahimi M., Geertsema E. M., Poelarends G. J. Curr. Opin. Chem. Biol., 2015, 25: 115.

[9]

Birolli W. G., Fonseca L. P., Porto A. L. M. Catal. Lett., 2017, 147(8): 1977.

[10]

Tian X. M., Zhang S. Q., Zheng L. Y. Enzyme Microb. Technol., 2016, 84: 32.

[11]

Zhang M. J., Li R., He Y. H., Guan Z. Catal. Commun., 2017, 98: 85.

[12]

Liang Y. R., Hu Y. J., Zhou X. H., Wu Q., Lin X. F. Tetrahedron Lett., 2017, 58(30): 2923.

[13]

Bihani M., Bora P. P., Verma A. K., Baruah R., Boruah H. P. D., Bez G. Bioorg. Med. Chem. Lett., 2015, 25(24): 5732.

[14]

Tang X. L., Liu J., Wang B., Yu H. W. World J. Microbiol. Biotechnol., 2011, 27(1): 129.

AI Summary AI Mindmap
PDF

142

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/