The [3+2] cycloaddition between various nitriles and trimethylsilyl azide proceeds smoothly in the presence of a Cu I catalyst in DMF/ MeOH, to give the corresponding 5-substituted 1H-tetrazoles in good to high yields. The reaction most probably proceeds through the in situ formation of a copper azi
β¦ LIBER β¦
Improved Synthesis of 5-Substituted 1H-Tetrazoles via the [3+2] Cycloaddition of Nitriles and Sodium Azide Catalyzed by Silica Sulfuric Acid
β Scribed by Du, Zhenting; Si, Changmei; Li, Youqiang; Wang, Yin; Lu, Jing
- Book ID
- 120430442
- Publisher
- Molecular Diversity Preservation International
- Year
- 2012
- Tongue
- English
- Weight
- 141 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1422-0067
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