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- Nitro derivatives of pyrrole, furan and 1H-tetrazole: ring or nitro bases?. M'hamed. Esseffar, Ester Quintanilla, Juan Z. Dávalos, José Luis M. Abboud, Otilia Mó, Manuel Yáñez
, New J. Chem.
, 2002
, 26
, 1567
- Photochemical transformations. Part VI. The photorearrangement of 2-nitrofuran and 2-nitropyrrole. R. Hunt, S. T. Reid
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 2527
- The photorearrangement of 2-nitrofuran and 2-nitropyrrole. R. Hunt, S. T. Reid
, J. Chem. Soc. D
, 1970
, 1576b
- Understanding the reactivity and selectivity of Diels–Alder reactions involving furans. Tiago Vinicius Alves, Israel Fernández
, Org. Biomol. Chem.
, 2023
, 21
, 7767
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5-Nitrofuran-2-ylmethyl group as a potential bioreductively activated
pro-drug system
. Jane M. Berry, Corrine Y. Watson, William J. D. Whish, Michael D. Threadgill
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 1147
- The boron trifluoride-catalysed reaction of furan derivatives with ethane-1,2-dithiol. B. Rindone, C. Scolastico
, J. Chem. Soc. C
, 1971
, 3339
- Design, synthesis, electrochemistry and anti-trypanosomatid hit/lead identification of nitrofuranylazines. Maryna Saayman, Christina Kannigadu, Janine Aucamp, Helena D. Janse van Rensburg, Cassiem Joseph, Andrew J. Swarts, David D. N'Da
, RSC Med. Chem.
, 2023
, 14
, 2012
- Tetrahydroisoquinoline based 5-nitro-2-furoic acid derivatives: a promising new approach for anti-tubercular agents. Adinarayana Nandikolla, Yogesh Mahadu Khetmalis, Guruvelli Padma Vijaya Sangeetha, Ala Chandu, Swati, Muthyala Murali Krishna Kumar, Vivek Sharma, Sankaranarayanan Murugesan, Kondapalli Venkata Gowri Chandra Sekhar
, New J. Chem.
, 2023
, 47
, 15378
- Ultrasensitive strips for the quadruple detection of nitrofuran metabolite residues. Wei Wu, Ning Sun, Simin Zhu, Xiaomei Li, Jitao Chen, Chunzhao Liu, Zhiyuan Fang, Qingli Yang
, RSC Adv.
, 2019
, 9
, 2812
- Synthesis and antimicrobial potential of nitrofuran–triazole congeners. Ahmed Kamal, S. M. Ali Hussaini, M. Lakshmi Sucharitha, Y. Poornachandra, Faria Sultana, C. Ganesh Kumar
, Org. Biomol. Chem.
, 2015
, 13
, 9388