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- 2-Nitropyrrole cross-coupling enables a second generation synthesis of the heronapyrrole antibiotic natural product family. Xiao-Bo Ding, Daniel P. Furkert, Margaret A. Brimble
, Chem. Commun.
, 2016
, 52
, 12638
- 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
- Universal base analogues and their applications in DNA sequencing technology. Feng Liang, Ying-Zhu Liu, Peiming Zhang
, RSC Adv.
, 2013
, 3
, 14910
- Monitoring the site-specific incorporation of dual fluorophore-quencher base analogues for target DNA detection by an unnatural base pair system. Rie Yamashige, Michiko Kimoto, Tsuneo Mitsui, Shigeyuki Yokoyama, Ichiro Hirao
, Org. Biomol. Chem.
, 2011
, 9
, 7504
- The photorearrangement of 2-nitrofuran and 2-nitropyrrole. R. Hunt, S. T. Reid
, J. Chem. Soc. D
, 1970
, 1576b
- 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
- Nitropyrrole natural products: isolation, biosynthesis and total synthesis. Xiao-Bo Ding, Margaret A. Brimble, Daniel P. Furkert
, Org. Biomol. Chem.
, 2016
, 14
, 5390
- Synthesis of substituted anilines via a gold-catalyzed three-component reaction. Hirofumi Ueda, Ryota Yamamoto, Minami Yamaguchi, Hidetoshi Tokuyama
, Org. Biomol. Chem.
, 2021
, 19
, 765
- The triplet state of N-(n-butyl)-5-nitro-2-furamide by laser flash photolysis. Spectrum, lifetime, energy and electron-transfer reactions. Luis J. A. Martins, Terence J. Kemp
, J. Chem. Soc., Faraday Trans. 1
, 1984
, 80
, 2509
- Exploring the synthetic potential of epoxide ring opening reactions toward the synthesis of alkaloids and terpenoids: a review. Madiha Hanif, Ameer Fawad Zahoor, Muhammad Jawwad Saif, Usman Nazeer, Kulsoom Ghulam Ali, Bushra Parveen, Asim Mansha, Aijaz Rasool Chaudhry, Ahmad Irfan
, RSC Adv.
, 2024
, 14
, 13100