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稳定笼 Aziridinium 离子的制备及其开环 Azaheterocycles 的合成
JoVE Journal
Chimica
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JoVE Journal Chimica
Preparation of Stable Bicyclic Aziridinium Ions and Their Ring-Opening for the Synthesis of Azaheterocycles
DOI:

11:45 min

August 22, 2018

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Capitoli

  • 00:04Titolo
  • 00:35Synthesis of (6R)-1-[(R)-1-Phenylethyl)-1-Azoniabicyclo[4.1.0]Heptane Tosylate
  • 02:49General Procedure for the Expansion of 1-Azoniabicyclo[4.1.0]Heptane Tosylate
  • 03:53Synthesis of (S)-1-[(R)-1-Phenylethyl]azepan-3-ol
  • 05:14Synthesis of [(2R,3R,4R)-3,4-Bis(Benzyloxy)-1-(S)-1-Phenylethyl)Piperidin-2-Yl]Methyl Acetate
  • 08:03Results: Synthesis and Characterization of Bicyclic Aziridinium Ions and its Ring Expansion to Azaheterocycles
  • 09:53Conclusion

Summary

Traduzione automatica

笼 aziridinium 离子, 如 1-azoniabicyclo [4.1. 0] 庚烷磺酸盐是由 2-[4-tolenesulfonyloxybutyl] 氮丙啶, 用于制备替代的 piperidines 和 azepanes 通过地-和立体环形膨胀与各种亲核试剂。这一高效的协议允许我们准备各种 azaheterocycles, 包括自然产品, 如 fagomine, febrifugine 模拟和 balanol。

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