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• Wang Nengzhong, Xiao Xiao, Liu Cheng‐Xiong, Yao Hui, Huang Nianyu, Zou Kun: Recent Advances in the Total Synthesis of Aspidosperma and Kopsia Alkaloids Using Tetracyclic Pyridocarbazoles as Versatile Building Blocks. Adv Synth Catal 2022, 364, 2479. <https://doi.org/10.1002/adsc.202200473>
• Wang Nengzhong, Jiang Xuefeng: Synthetic Approaches to Tricyclic Aminoketones in the Total Synthesis of Aspidosperma and Kopsia Alkaloids. The Chemical Record 2021, 21, 295. <https://doi.org/10.1002/tcr.202000131>
• Yang Lu, Huang Siwen, Huang Rongkang, Hou Anbin, Zhang Sen, Su Hongwei, Ding Xiaohong, Lin Bin, Cheng Maosheng, Liu Yongxiang: Total Syntheses of Aspidospermidine, N-Methylaspidospermidine, N-Acetylaspidospermidine, and Aspidospermine via a Tandem Cyclization of Tryptamine-Ynamide. Org. Lett. 2021, 23, 6471. <https://doi.org/10.1021/acs.orglett.1c02287>
• Varga Szilárd, Angyal Péter, Martin Gábor, Egyed Orsolya, Holczbauer Tamás, Soós Tibor: Total Syntheses of (−)‐Minovincine and (−)‐Aspidofractinine through a Sequence of Cascade Reactions. Angewandte Chemie 2020, 132, 13649. <https://doi.org/10.1002/ange.202004769>
• Varga Szilárd, Angyal Péter, Martin Gábor, Egyed Orsolya, Holczbauer Tamás, Soós Tibor: Total Syntheses of (−)‐Minovincine and (−)‐Aspidofractinine through a Sequence of Cascade Reactions. Angew Chem Int Ed 2020, 59, 13547. <https://doi.org/10.1002/anie.202004769>
• Martin Gábor, Angyal Péter, Egyed Orsolya, Varga Szilárd, Soós Tibor: Total Syntheses of Dihydroindole Aspidosperma Alkaloids: Reductive Interrupted Fischer Indolization Followed by Redox Diversification. Org. Lett. 2020, 22, 4675. <https://doi.org/10.1021/acs.orglett.0c01472>
• Bingul Murat, Saglam Mehmet F., Kandemir Hakan, Boga Mehmet, Sengul Ibrahim F.: Synthesis of indole-2-carbohydrazides and 2-(indol-2-yl)-1,3,4-oxadiazoles as antioxidants and their acetylcholinesterase inhibition properties. Monatsh Chem 2019, 150, 1553. <https://doi.org/10.1007/s00706-019-02462-y>
• Nazir Majid, Abbasi Muhammad Athar, Aziz-ur-Rehman, Siddiqui Sabahat Zahra, Khan Khalid Mohammed, Kanwal, Salar Uzma, Shahid Muhammad, Ashraf Muhammad, Arif Lodhi Muhammad, Ali Khan Farman: New indole based hybrid oxadiazole scaffolds with N-substituted acetamides: As potent anti-diabetic agents. Bioorganic Chemistry 2018, 81, 253. <https://doi.org/10.1016/j.bioorg.2018.08.010>
• Xu Zhengren, Wang Qian, Zhu Jieping: Metamorphosis of cycloalkenes for the divergent total synthesis of polycyclic indole alkaloids. Chem. Soc. Rev. 2018, 47, 7882. <https://doi.org/10.1039/C8CS00454D>
• Deka Bhaskar, Baruah Pranjal K., Deb Mohit L.: Multi-component synthesis of 3-substituted indoles and their cyclisation to α-carbolines via I2-promoted intramolecular C2 oxidative amination/aromatisation at room temperature. Org. Biomol. Chem. 2018, 16, 7806. <https://doi.org/10.1039/C8OB02362J>
• Nazir Majid, Abbasi Muhammad Athar, Aziz-ur-Rehman Aziz-ur-Rehman, Siddiqui Sabahat Zahra, Raza Hussain, Hassan Mubashir, Ali Shah Syed Adnan, Shahid Muhammad, Seo Sung-Yum: Novel indole based hybrid oxadiazole scaffolds with N-(substituted-phenyl)butanamides: synthesis, lineweaver–burk plot evaluation and binding analysis of potent urease inhibitors. RSC Adv. 2018, 8, 25920. <https://doi.org/10.1039/C8RA04987D>
• Deb Mohit L., Pegu Choitanya Dev, Deka Bhaskar, Dutta Prantu, Kotmale Amol S., Baruah Pranjal K.: Brønsted‐Acid‐Mediated Divergent Reactions of Betti Bases with Indoles: An Approach to Chromeno[2,3‐b]indoles through Intramolecular Dehydrogenative C2‐Alkoxylation of Indole. Eur J Org Chem 2016, 2016, 3441. <https://doi.org/10.1002/ejoc.201600546>
• Omidi Mehdi, Amrollahi Mohammad Ali: Facile synthesis of 3-substituted indoles containing highly polarized double bonds. Comptes Rendus. Chimie 2016, 20, 549. <https://doi.org/10.1016/j.crci.2016.09.004>
• Rajesh U. Chinna, Kholiya Rohit, Thakur Anuj, Rawat Diwan S.: [TBA][Gly] ionic liquid promoted multi-component synthesis of 3-substituted indoles and indolyl-4H-chromenes. Tetrahedron Letters 2015, 56, 1790. <https://doi.org/10.1016/j.tetlet.2015.02.058>
• Cao Liang-Liang, Li Xu-Ni, Meng Fan-Yan, Jiang Guo-Fang: Pd-catalyzed addition of boronic acids to vinylogous imines: a convenient approach to 3-sec-alkyl substituted indoles. Tetrahedron Letters 2012, 53, 3873. <https://doi.org/10.1016/j.tetlet.2012.05.056>
• Larghi Enrique L., Kaufman Teodoro S.: Synthesis of Oxacycles Employing the Oxa‐Pictet–Spengler Reaction: Recent Developments and New Prospects. Eur J Org Chem 2011, 2011, 5195. <https://doi.org/10.1002/ejoc.201100271>
• Jafarpour Maasoumeh, Rezaeifard Abdolreza, Gorzin Ghorbanali: Enhanced catalytic activity of Zr(IV) complex with simple tetradentate Schiff base ligand in the clean synthesis of indole derivatives. Inorg Chem Commun 2011, 14, 1732. <https://doi.org/10.1016/j.inoche.2011.07.017>
• Cao Liang-Liang, Wang Duo-Sheng, Jiang Guo-Fang, Zhou Yong-Gui: An efficient route to 2,3-disubstituted indoles via reductive alkylation using H2 as reductant. Tetrahedron Letters 2011, 52, 2837. <https://doi.org/10.1016/j.tetlet.2011.03.099>
• Bringmann Gerhard, Gulder Tanja, Gulder Tobias A. M., Breuning Matthias: Atroposelective Total Synthesis of Axially Chiral Biaryl Natural Products. Chem. Rev. 2011, 111, 563. <https://doi.org/10.1021/cr100155e>
• Hájíček Josef: Recent developments in syntheses of the post-secodine indole alkaloids. Part III: Rearranged alkaloid types. Collect. Czech. Chem. Commun. 2011, 76, 2023. <https://doi.org/10.1135/cccc2011099>
• Bartoli Giuseppe, Bencivenni Giorgio, Dalpozzo Renato: Organocatalytic strategies for the asymmetric functionalization of indoles. Chem. Soc. Rev. 2010, 39, 4449. <https://doi.org/10.1039/b923063g>
• Hajicek Josef: A Review on Recent Developments in Syntheses of the Post‐Secodine Indole Alkaloids. Part 2. Modified Alkaloid Types. ChemInform 2007, 38. <https://doi.org/10.1002/chin.200748229>