Synthesis of 5-substituted 1H-tetrazoles by clean cabbage like silver crystals
Publish place: 27th Iranian Seminar on Organic Chemistry
Publish Year: 1398
نوع سند: مقاله کنفرانسی
زبان: English
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شناسه ملی سند علمی:
ISOC27_305
تاریخ نمایه سازی: 19 اسفند 1399
Abstract:
Tetrazoles are synthetic heterocyclic compounds having one carbon and four nitrogen atoms in a five-membered ring.1 They have widespread applications in materials science,2 and medicinal chemistry.3 Moreover, they can be served as lipophilic spacers and carboxylic acid substitutes.4 One of the most significant aims of tetrazoles chemistry is searching for a new synthetic method as well as improvement of previous procedures. The most versatile used method for the syntheses of 5-substituted 1H-tetrazoles is [3+2] cycloaddition of nitriles and azide anion in the presence of various catalysts and solvent conditions. Several organic, inorganic, homogeneous, and heterogeneous catalysts have been used for this purpose. Herein we introduced our process as a highly efficient method for conversion of aldehydes into the corresponding 5-substituted 1H-tetrazoles using clean cabbage like silver crystals as reusable catalyst (Fig.1).
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Authors
Roghayeh Heiran
Department of Chemistry, Estahban higher education center, Estahban, Iran. Department of Chemistry, Faculty of Science, Shiraz University, Shiraz, Iran
Fatemeh Sedaghati,
Department of Chemistry, Estahban higher education center, Estahban, Iran
Mohammad Amin Kamali
Department of Chemistry, Estahban higher education center, Estahban, Iran