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Alkaloids of Uncaria pteropoda. Isolation and structures of pteropodine and isopteropodine. K. C. Chan, F. Morsingh, G. B. Yeoh , J. Chem. Soc. C , 1966 , 2245

176. The chemistry of the Mitragyna genus. Part I. G. M. Badger, J. W. Cook, P. A. Ongley , J. Chem. Soc. , 1950 , 867

Analysis of the kinetics of isomerization of spiro oxindole alkaloids. Gerhard Laus, Dagmar Brössner, Gilbert Senn, Klaus Wurst , J. Chem. Soc., Perkin Trans. 2 , 1996 , 1931

Collective formal synthesis of (±)-rhynchophylline and homologues. Jun Xu, Li-Dong Shao, Xin Shi, Jian Ren, Chengfeng Xia, Qin-Shi Zhao , RSC Adv. , 2016 , 6 , 63131

Evaluation of extraction methods for pharmacologically active compounds from anticonvulsant traditional Chinese medicines: Gou Teng, Tian Ma, Jiang Can using DART-TOF-MS. Kimberly N. Karin, Justin L. Poklis, Michelle R. Peace , Anal. Methods , 2021 , 13 , 884

The stereochemistry of formosanine (uncarine B) and uncarine A. A. F. Beecham, N. K. Hart, S. R. Johns, J. A. Lamberton , Chem. Commun. (London) , 1967 , 535

Recent progress in the chemistry of indole alkaloids and mould metabolites. J. E. Saxton , Nat. Prod. Rep. , 1985 , 2 , 49

Novel diastereoselective synthesis of spiropyrrolidine-oxindole derivatives as anti-breast cancer agents. Atul Kumar, Garima Gupta, Suman Srivastava, Ajay Kumar Bishnoi, Ruchi Saxena, Ruchir Kant, Ranjana S. Khanna, Prakas R. Maulik, Anila Dwivedi , RSC Adv. , 2013 , 3 , 4731

Oleic acid: a benign Brønsted acidic catalyst for densely substituted indole derivative synthesis. Asaithampi Ganesan, Jagatheeswaran Kothandapani, Jagadeesh Babu Nanubolu, Subramaniapillai Selva Ganesan , RSC Adv. , 2015 , 5 , 28597

The mechanism and diastereoselectivity in the formation of trifluoromethyl-containing spiro[pyrrolidin-3,2′-oxindole] by a catalyst-free and mutually activated [3+2]-cycloaddition reaction: a theoretical study. Xingyu Wang, Yan Zhang, Yongsheng Yang, Ying Xue , New J. Chem. , 2020 , 44 , 17465