番木鳖碱structure of Strychnine , Brucine and Vomicine. Progress in Organic Chemistry. 1952, 1: 2. Nicolaou KC, Sorensen EJ. Classics in Total Synthesis : Targets
三仲丁基硼氢化锂and G. Pairaudeau. Synthesis applications of cationic aza-Cope rearrangements. 26. Enantioselective total synthesis of (-)-strychnine . J. Am. Chem. Soc
福山吲哚合成1021/ja0177049. Kaburagi, Y; Tokuyama, H; Fukuyama, T. Total Synthesis of (-)-Strychnine . J. Am. Chem. Soc. 2004, 126 (33): 10246–10247. PMID 15315428
三枝-伊藤氧化反应 ; Shimizu, S.; Zhong, D.; Shibasaki, M., Enantioselective Total Synthesis of (−)-Strychnine Using the Catalytic Asymmetric Michael Reaction and Tandem
六氟锑酸铜 with Indoles: A General Protocol for the Formal Total Synthesis of (±)-Strychnine and the Total Synthesis of (±)-Akuammicine. Angewandte Chemie International