Atul J. Dolas, Arun Patel, Imtiyaz A. Shah, Jyothi Yadav, Eldhose Iype and Indresh Kumar
Org. Biomol. Chem., 2025,23, 2523-2538
Abstract
Asymmetric synthesis of 2,2-disubstituted indolin-3-ones has attracted much attention due to their presence in many important compounds. Herein, we discuss this unit's current state of asymmetric synthetic methods under different catalytic systems.
Roman A. Irgashev and Alexander S. Steparuk
Org. Biomol. Chem., 2024,22, 6174-6180
Abstract
A single protocol for the construction of various selenopheno[3,2-b]indole-cored molecules from appropriate 3-aminoselenophene substrates using Fischer indolization was elaborated in this study.
Le-Mao Yu, Haojin Chen, Wenjing Fang, Ruonan Cai, Yi Tao, Yong Li and Huaping Dong
Org. Biomol. Chem., 2024,22, 7074-7091
Abstract
The present review highlights the dearomatization of indoles by oxidizing C–H bonds for constructing oxindoles skeletons. Various synthetic approaches have been summarized followed by their applications in indole alkaloids and bioactive compounds.
Suven Das
New J. Chem., 2023,47, 13729-13775
Abstract
The present review summarizes recent (2019–mid-2023) efforts towards the construction of the indole core via transition-metal-free methods.
Carl Bowman, Maxime Denis and Sylvain Canesi
Chem. Commun., 2025,61, 5563-5576
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Abstract
Synthesis of unnatural indoles and indolines as key steps in the total synthesis of complex natural products, a recent review.