
European Journal of Medicinal Chemistry p. 213 - 220 (1987)
Update date:2022-08-02
Topics:
Bilger, Christine
Demerseman, Pierre
Buisson, Jean-Pierre
Royer, Rene
Gayral, Philippe
Fourniat, Jacky
Modifications of biological activity following addition of a second nitrofuran cycle to nitroarenofuran homocycles. 2,7-dinitro-benzo<1,2-b:4,3-b'>difuran is prepared by direct nitration of 2-nitro-benzo<1,2-b:4,3-b'>difuran, whereas the corresponding derivatives nitrated in the α-position of each heterocycle of naphtho<2,1-b:7,6-b'>difuran, naphtho<2,1-b:6,5-b'>difuran, naphtho<1,2-b:6,5-b'>difuran and anthra<2,1-b:6,5-b'>difuran are obtained by condensation of bromonitromethane with appropriate bis-(ortho-hydroxyformyl) naphthalenes or anthracene.These dinitroarenodifurans are generally more efficient against bacteria and protozoa than 2-nitro-benzofuran itself and 2-nitro-naphthofurans.Keywords - arenodifurans/ nitroarenofurans/ anti-bacterial/ protozoicide
View MoreContact:18710867521(wechat)
Address:Rm10516,Galaxy Tech Building #2,No.25 Tangyan Rd,Hi-Tech Zone,Xi'an, China
Huangshi Shennong Chemical Technology Co., Ltd
Contact:+86-714-3072290
Address:Eastern industrial park , Tieshan district , Huangshi city ,Hubei province , China
Jintan City Mego Chemical Co., Ltd
Contact:+86-0519-82814387
Address:23# Dengguan Town, Jintan, Jiangsu Province, China
Beijing Mashi Fine Chemical Co.,Ltd.
Contact:+86-10-61271592
Address:Room 506, Section B, Kaichi Mansion, Industrial Development
Contact:+1 (647) 918 5848
Address:2343 BRIMLEY RD., Suite 250
Doi:10.1021/jf1023643
(2010)Doi:10.1135/cccc19982075
(1998)Doi:10.1016/j.tet.2008.11.071
(2009)Doi:10.1007/BF00475469
(1987)Doi:10.1002/anie.201609695
(2017)Doi:10.1021/acs.jmedchem.0c00816
(2020)