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- Studies towards streptonigrinoids: formal synthesis of lavendamycin methyl ester. Marco A. Ciufolini, Michael J. Bishop
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- Quinoline, quinazoline and acridone alkaloids. Joseph P. Michael
, Nat. Prod. Rep.
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- Recent progress in the chemistry of non-monoterpenoid indole alkaloids. M. Ihara, K. Fukumoto
, Nat. Prod. Rep.
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- 2-Aroylquinoline-5,8-diones as potent anticancer agents displaying tubulin and heat shock protein 90 (HSP90) inhibition. Kunal Nepali, Sunil Kumar, Hsiang-Ling Huang, Fei-Chiao Kuo, Cheng-Hsin Lee, Ching-Chuan Kuo, Teng-Kuang Yeh, Yu-Hsuan Li, Jang-Yang Chang, Jing-Ping Liou, Hsueh-Yun Lee
, Org. Biomol. Chem.
, 2016
, 14
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- Simple indole alkaloids and those with a non-rearranged monoterpenoid unit. Minoru Ishikura, Takumi Abe, Tominari Choshi, Satoshi Hibino
, Nat. Prod. Rep.
, 2013
, 30
, 694
- The genus Micromonospora as a model microorganism for bioactive natural product discovery. Mohamed S. Hifnawy, Mohamed M. Fouda, Ahmed M. Sayed, Rabab Mohammed, Hossam M. Hassan, Sameh F. AbouZid, Mostafa E. Rateb, Alexander Keller, Martina Adamek, Nadine Ziemert, Usama Ramadan Abdelmohsen
, RSC Adv.
, 2020
, 10
, 20939
- BF3·Et2O mediated one-step synthesis of N-substituted-1,2-dihydropyridines, indenopyridines and 5,6-dihydroisoquinolines. C. T. Fathimath Salfeena, K. T. Ashitha, B. S. Sasidhar
, Org. Biomol. Chem.
, 2016
, 14
, 10165
- Versatile tools in the construction of substituted 2,2′-bipyridines—cross-coupling reactions with tin, zinc and boron compounds. Marko Hapke, Lars Brandt, Arne Lützen
, Chem. Soc. Rev.
, 2008
, 37
, 2782
- Construction of heterocyclic structures by trivalent cerium salts promoted bond forming reactions. Roberta Properzi, Enrico Marcantoni
, Chem. Soc. Rev.
, 2014
, 43
, 779
- Synthesis and biological evaluation of 1,4-naphthoquinones and quinoline-5,8-diones as antimalarial and schistosomicidal agents. Don Antoine Lanfranchi, Elena Cesar-Rodo, Benoît Bertrand, Hsin-Hung Huang, Latasha Day, Laure Johann, Mourad Elhabiri, Katja Becker, David L. Williams, Elisabeth Davioud-Charvet
, Org. Biomol. Chem.
, 2012
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, 6375