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- A general strategy for the synthesis of indoloquinolizine alkaloids via a cyanide-catalyzed imino-Stetter reaction. Eunjoon Park, Cheol-Hong Cheon
, Org. Biomol. Chem.
, 2017
, 15
, 10265
- Synthesis, biological evaluation and docking studies of some novel isatin-3-hydrazonothiazolines. Maqbool Ahmad, Humayun Pervez, Sumera Zaib, Muhammad Yaqub, Muhammad Moazzam Naseer, Shafi Ullah Khan, Jamshed Iqbal
, RSC Adv.
, 2016
, 6
, 60826
- 3-Substituted 2-phenyl-indoles: privileged structures for medicinal chemistry. Henrik Johansson, Tanja Bøgeløv Jørgensen, David E. Gloriam, Hans Bräuner-Osborne, Daniel Sejer Pedersen
, RSC Adv.
, 2013
, 3
, 945
- Diastereoselective synthesis of functionalised carbazoles via a sequential Diels–Alder/ene reaction strategy. Joseph Cowell, Matokah Abualnaja, Stephanie Morton, Ruth Linder, Faye Buckingham, Paul G. Waddell, Michael R. Probert, Michael J. Hall
, RSC Adv.
, 2015
, 5
, 16125
- Doubly prenylated tryptamines: cytotoxicity, antimicrobial activity and cyclisation to the marine natural product flustramine A. Santosh Kumar Adla, Florenz Sasse, Gerhard Kelter, Heinz-Herbert Fiebig, Thomas Lindel
, Org. Biomol. Chem.
, 2013
, 11
, 6119
- Antitumour indolequinones: synthesis and activity against human pancreatic cancer cells. Martyn Inman, Andrea Visconti, Chao Yan, David Siegel, David Ross, Christopher J. Moody
, Org. Biomol. Chem.
, 2014
, 12
, 4848
- Regioselective, one-pot, multi-component, green synthesis of substituted benzo[c]pyrazolo[2,7]naphthyridines. Abida Ashraf, Zahid Shafiq, Khalid Mahmood, Muhammad Yaqub, Waqar Rauf
, RSC Adv.
, 2020
, 10
, 5938
- Synthesis and biological activity of novel bis-indole inhibitors of bacterial transcription initiation complex formation. Marcin Mielczarek, Ruth V. Devakaram, Cong Ma, Xiao Yang, Hakan Kandemir, Bambang Purwono, David StC. Black, Renate Griffith, Peter J. Lewis, Naresh Kumar
, Org. Biomol. Chem.
, 2014
, 12
, 2882
- A synthetic route to 1,4-disubstituted tetrahydro-β-carbolines and tetrahydropyranoindoles via ring-opening/Pictet–Spengler reaction of aziridines and epoxides with indoles/aldehydes. Imtiyaz Ahmad Wani, Gaurav Goswami, Sahid Sk, Abhijit Mal, Masthanvali Sayyad, Manas K. Ghorai
, Org. Biomol. Chem.
, 2020
, 18
, 272
- Metal-free regioselective C-3 acetoxylation of N-substituted indoles: crucial impact of nitrogen-substituent. Vineeta Soni, Ulhas N. Patel, Benudhar Punji
, RSC Adv.
, 2015
, 5
, 57472