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Journals / Turkish Journal of Chemistry / 2014 / Cilt: 38 - Sayı: 1

Self-condensation reactions of acyl phosphonates: synthesis of tertiary O-protected a-hydroxyphosphonates

Serkan EYMUR
Mehmet GÖLLÜ
Ayhan Sıtkı DEMİR
Pages
164–171
Publication Date
2014-05-18
DOI
—
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AI Summary & Key Takeaways

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

The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.
📊
Key Findings & Data:The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.
💡
Conclusion & Impact:The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Acyl phosphonates · tertiary a-hydroxy phosphonates · phosphonate-phosphate rearrangement

Abstract

The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.

Özet

The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.

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Cite This Article

EYMUR, S., GÖLLÜ, M., DEMİR, A. S. (2014). Self-condensation reactions of acyl phosphonates: synthesis of tertiary O-protected a-hydroxyphosphonates. Turkish Journal of Chemistry, Cilt: 38 - Sayı: 1, 164–171. https://ajindex.com/articles/174454

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