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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
Alcohols and phenols were tetrahydropyranylated in the presence of 2,4,6-trichloro[1,3,5]triazine in good to excellent yields in acetonitrile.
📌 3 Key Takeaways
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Objective & Hypothesis:Alcohols and phenols were tetrahydropyranylated in the presence of 2,4,6-trichloro[1,3,5]triazine in good to excellent yields in acetonitrile.
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Key Findings & Data:Alcohols and phenols were tetrahydropyranylated in the presence of 2,4,6-trichloro[1,3,5]triazine in good to excellent yields in acetonitrile.
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Conclusion & Impact:Alcohols and phenols were tetrahydropyranylated in the presence of 2,4,6-trichloro[1,3,5]triazine in good to excellent yields in acetonitrile.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:6- Trichloro[1 · 5]triazine (TT) · cyanuric chloride (CC)
Abstract
Alcohols and phenols were tetrahydropyranylated in the presence of 2,4,6-trichloro[1,3,5]triazine in good to excellent yields in acetonitrile.
Özet
Alcohols and phenols were tetrahydropyranylated in the presence of 2,4,6-trichloro[1,3,5]triazine in good to excellent yields in acetonitrile.
Keywords
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Cite This Article
AKHLAGHINIA, B., ROOHI, E. (2007). Efficient Method for Tetrahydropyranylation of Phenols and Alcohols Using 2,4,6-Trichloro[1,3,5]triazine. Turkish Journal of Chemistry, Cilt: 31 - Sayı: 1, 83–88. https://ajindex.com/articles/217993