Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1986, 51, 1731-1742
https://doi.org/10.1135/cccc19861731

(-)-Strempeliopine, stereoselective total synthesis and the determination of absolute configuration

Josef Hájíček and Jan Trojánek

Research Institute for Pharmacy and Biochemistry, 194 04 Prague 9

Crossref Cited-by Linking

  • Zhang Xiangyu: Vallesamidine and schizozygane alkaloids: rearranged monoterpene indole alkaloids and synthetic endeavours. Nat. Prod. Rep. 2024. <https://doi.org/10.1039/D3NP00048F>
  • Zhang Zeliang, Qian Xiao, Gu Yucheng, Gui Jinghan: Controllable skeletal reorganizations in natural product synthesis. Nat. Prod. Rep. 2024, 41, 251. <https://doi.org/10.1039/D3NP00066D>
  • Otogo N’Nang Elvis, Cauchie Gaëla, Retailleau Pascal, Agnandji Selidji Todagbe, Gallard Jean-François, Mouray Elisabeth, Grellier Philippe, Champy Pierre, Le Pogam Pierre, Beniddir Mehdi A.: From the Spectroscopic Reassessment of Authentic Alkaloid Samples to the Molecular Networking-Guided Discovery of Criophylline-Related Analogues from Callichilia inaequalis. J. Nat. Prod. 2023, 86, 1202. <https://doi.org/10.1021/acs.jnatprod.2c01084>
  • Heravi Majid. M., Nazari Azadeh: Samarium(ii) iodide-mediated reactions applied to natural product total synthesis. RSC Adv. 2022, 12, 9944. <https://doi.org/10.1039/D1RA08163B>
  • Zeng Xianhuang, Boger Dale L.: Total Synthesis of (−)-Strempeliopine. J. Am. Chem. Soc. 2021, 143, 12412. <https://doi.org/10.1021/jacs.1c06913>
  • Zhou Wenqiang, Zhou Tao, Tian Mengxing, Jiang Yan, Yang Jiaojiao, Lei Shuai, Wang Qi, Zhang Chongzhou, Qiu Hanyue, He Ling, Wang Zhen, Deng Jun, Zhang Min: Asymmetric Total Syntheses of Schizozygane Alkaloids. J. Am. Chem. Soc. 2021, 143, 19975. <https://doi.org/10.1021/jacs.1c10279>
  • Zhou Qilong, Dai Xiang, Song Hao, He Huan, Wang Xiaobei, Liu Xiao-Yu, Qin Yong: Concise syntheses of eburnane indole alkaloids. Chem. Commun. 2018, 54, 9510. <https://doi.org/10.1039/C8CC05374J>
  • 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>
  • Bobeck Drew R., Lee Hyoung Ik, Flick Andrew C., Padwa Albert: Application of Cross-Conjugated Heteroaromatic Betaines to the Synthesis of the Schizozygane Alkaloid (±)-Strempeliopine. J. Org. Chem. 2009, 74, 7389. <https://doi.org/10.1021/jo901336z>
  • Stephens Philip J., Pan Jian-Jung, Devlin Frank J., Urbanová Marie, Hájíček Josef: Determination of the Absolute Configurations of Natural Products via Density Functional Theory Calculations of Vibrational Circular Dichroism, Electronic Circular Dichroism and Optical Rotation:  The Schizozygane Alkaloid Schizozygine. J. Org. Chem. 2007, 72, 2508. <https://doi.org/10.1021/jo062567p>
  • Pilarčík Tomáš, Havlíček Jaroslav, Hájíček Josef: Towards schizozygine: synthesis of 15α-hydroxystrempeliopine. Tetrahetron Lett 2005, 46, 7909. <https://doi.org/10.1016/j.tetlet.2005.09.098>
  • Hájíček Josef, Taimr Jan, Buděšínský Miloš: Revised structure of isoschizogamine. Tetrahetron Lett 1998, 39, 505. <https://doi.org/10.1016/S0040-4039(97)10588-3>
  • HAJICEK J., TROJANEK J.: ChemInform Abstract: Alkaloids. Part 52. (‐)‐Strempeliopine. Stereoselective Total Synthesis and the Determination of Absolute Configuration. ChemInform 1987, 18. <https://doi.org/10.1002/chin.198701316>