Journals / Hacettepe Journal of Biology and Chemistry / 2003 / Cilt: 32 - Sayı:

Studies on the synthesis of tetracyclic indole alkaloids. Synthesis of azocino [4,3-b] indole framework

Pages
113–121
Publication Date
2022-10-17
DOI
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

The structures were confirmed by NMR, MS, FT-IR techniques and elemental analysis.

📌 3 Key Takeaways

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Objective & Hypothesis:The synthesis of the compound 10 which has hexahydro-l,5-methanoazocino[4,3-b]indole structure for the synthesis of pentacyclic strychnos type of alkaloids (tubifolin and tubifolidine) was described.
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Key Findings & Data:Many new tetrahydrocarbazol intermediates and hexahydro-1,5-methanoazocino[4,3-b]indole derivative (5, 6a, 6b, 6c, 6d, 7, 8,10) have also been synthesized.
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Conclusion & Impact:The structures were confirmed by NMR, MS, FT-IR techniques and elemental analysis.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

The synthesis of the compound 10 which has hexahydro-l,5-methanoazocino[4,3-b]indole structure for the synthesis of pentacyclic strychnos type of alkaloids (tubifolin and tubifolidine) was described. Many new tetrahydrocarbazol intermediates and hexahydro-1,5-methanoazocino[4,3-b]indole derivative (5, 6a, 6b, 6c, 6d, 7, 8,10) have also been synthesized. The structures were confirmed by NMR, MS, FT-IR techniques and elemental analysis.

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Cite This Article

PATIR, S., OKAY, G., ERGÜN, Y. (2022). Studies on the synthesis of tetracyclic indole alkaloids. Synthesis of azocino [4,3-b] indole framework. Hacettepe Journal of Biology and Chemistry, Cilt: 32 - Sayı:, 113–121. https://ajindex.com/articles/529426

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References (1)

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