Journals / Turkish Journal of Chemistry / 2009 / Cilt: 33 - Sayı: 2

A Mild Method for the Cleavage of Ketals Using IBX

Pages
209–214
Publication Date
2009-02-01
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

A variety of functional groups showed no interference under these conditions except vinyl bromides, which, in fact, inhibits the single electron transfer to IBX.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Investigation on the total synthesis of batrachotoxin 1 revealed that the cyclic ketals could be cleaved to ketone with IBX in DMSO at 70-81 °C under very mild conditions.
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Key Findings & Data:Investigation on the total synthesis of batrachotoxin 1 revealed that the cyclic ketals could be cleaved to ketone with IBX in DMSO at 70-81 °C under very mild conditions.
💡
Conclusion & Impact:A variety of functional groups showed no interference under these conditions except vinyl bromides, which, in fact, inhibits the single electron transfer to IBX.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Deprotection · ketal · IBX

Abstract

Investigation on the total synthesis of batrachotoxin 1 revealed that the cyclic ketals could be cleaved to ketone with IBX in DMSO at 70-81 °C under very mild conditions. A variety of functional groups showed no interference under these conditions except vinyl bromides, which, in fact, inhibits the single electron transfer to IBX.

Özet

Investigation on the total synthesis of batrachotoxin 1 revealed that the cyclic ketals could be cleaved to ketone with IBX in DMSO at 70-81 °C under very mild conditions. A variety of functional groups showed no interference under these conditions except vinyl bromides, which, in fact, inhibits the single electron transfer to IBX.

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Cite This Article

RAZA, A. R. (2009). A Mild Method for the Cleavage of Ketals Using IBX. Turkish Journal of Chemistry, Cilt: 33 - Sayı: 2, 209–214. https://ajindex.com/articles/184957

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