One pot 'click'reaction: Cu II–hydrotalcite catalyzed tandem synthesis of β-hydroxy triazoles via regioselective opening of epoxide followed by [3+ 2] cycloaddition

AN Prasad, B Thirupathi, G Raju, R Srinivas… - Catalysis Science & …, 2012 - pubs.rsc.org
AN Prasad, B Thirupathi, G Raju, R Srinivas, BM Reddy
Catalysis Science & Technology, 2012pubs.rsc.org
A novel copper (II) hydrotalcite catalyst has been investigated for its use in the cascade
synthesis of β-hydroxy triazoles. It is found to be a dynamic catalyst for regioselective
organic synthesis in water. The copper (II) hydrotalcite catalyst, in various Cu: Al molar
ratios, was prepared by adopting a coprecipitation method and characterized using different
techniques. The three component (epoxides, sodium azide and terminal alkynes) reactions
under investigation were performed in water at ambient temperature without any additives …
A novel copper (II) hydrotalcite catalyst has been investigated for its use in the cascade synthesis of β-hydroxy triazoles. It is found to be a dynamic catalyst for regioselective organic synthesis in water. The copper (II) hydrotalcite catalyst, in various Cu : Al molar ratios, was prepared by adopting a coprecipitation method and characterized using different techniques. The three component (epoxides, sodium azide and terminal alkynes) reactions under investigation were performed in water at ambient temperature without any additives. The formation of 2-azido alcohol, generated in situ, was observed to be the key step in the [3+2] cycloaddition of the click reaction. The optimized reaction procedures described herein are not only regioenriched and high yielding but also eco-friendly.
The Royal Society of Chemistry
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