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- Synthesis, cytotoxic and urease inhibitory activities of some novel isatin-derived bis-Schiff bases and their copper(ii) complexes. Humayun Pervez, Maqbool Ahmad, Sumera Zaib, Muhammad Yaqub, Muhammad Moazzam Naseer, Jamshed Iqbal
, Med. Chem. Commun.
, 2016
, 7
, 914
- Synthesis and evaluation of metallocene containing methylidene-1,3-dihydro-2H-indol-2-ones as kinase inhibitors. John Spencer, Jahangir Amin, Samantha K. Callear, Graham J. Tizzard, Simon J. Coles, Peter Coxhead, Matthew Guille
, Metallomics
, 2011
, 3
, 600
- Iron-catalyzed C(sp3)–H functionalization of methyl azaarenes: a green approach to azaarene-substituted α- or β-hydroxy carboxylic derivatives and 2-alkenylazaarenes. Danwei Pi, Kun Jiang, Haifeng Zhou, Yuebo Sui, Yasuhiro Uozumi, Kun Zou
, RSC Adv.
, 2014
, 4
, 57875
- The interaction of molybdenum pentachloride with carbonyl compounds. Fabio Marchetti, Guido Pampaloni, Stefano Zacchini
, Dalton Trans.
, 2013
, 42
, 2477
- Synthesis and evaluation of oxindoles as promising inhibitors of the immunosuppressive enzyme indoleamine 2,3-dioxygenase 1. Saurav Paul, Ashalata Roy, Suman Jyoti Deka, Subhankar Panda, Gopal Narayan Srivastava, Vishal Trivedi, Debasis Manna
, Med. Chem. Commun.
, 2017
, 8
, 1640
- Ru-Catalyzed dehydrogenative synthesis of antimalarial arylidene oxindoles. Girish Singh Bisht, Akanksha M. Pandey, Moreshwar B. Chaudhari, Sandip G. Agalave, Abhishek Kanyal, Krishanpal Karmodiya, Boopathy Gnanaprakasam
, Org. Biomol. Chem.
, 2018
, 16
, 7223
- Friedel–Crafts alkylations of electron-rich aromatics with 3-hydroxy-2-oxindoles: scope and limitations. Lakshmana K. Kinthada, Santanu Ghosh, K. Naresh Babu, Mohd. Sharique, Soumava Biswas, Alakesh Bisai
, Org. Biomol. Chem.
, 2014
, 12
, 8152
- Metal-catalyzed rearrangements of 3-allenyl 3-hydroxyindolin-2-ones in the presence of halogenated reagents. Benito Alcaide, Pedro Almendros, Amparo Luna, Natividad Prieto
, Org. Biomol. Chem.
, 2013
, 11
, 1216
- Structural and biological investigation of ferrocene-substituted 3-methylidene-1,3-dihydro-2H-indol-2-ones. John Spencer, Andrew P. Mendham, Arun K. Kotha, Simon C. W. Richardson, Elizabeth A. Hillard, Gérard Jaouen, Louise Male, Michael B. Hursthouse
, Dalton Trans.
, 2009
, 918
- Acid-catalyzed reactions of 3-hydroxy-2-oxindoles with electron-rich substrates: synthesis of 2-oxindoles with all-carbon quaternary center. Lakshmana K. Kinthada, Santanu Ghosh, Subhadip De, Subhajit Bhunia, Dhananjay Dey, Alakesh Bisai
, Org. Biomol. Chem.
, 2013
, 11
, 6984