Cycloadditions to [60]fullerene using microwave irradiation: A convenient and expeditious procedure
โ Scribed by Pilar de la Cruz; Antonio de la Hoz; Fernando Langa; Beatriz Illescas; Nazario Martin
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 514 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0040-4020
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๐ SIMILAR VOLUMES
The reactions of aliphatic alcohols with p-toluenesulfinic acid are accelerated by microwave irradiation under solvent-free conditions in the presence of silica gel to afford a high yielding synthesis of p-toluenesulfinate esters.
New ct-hetero ~-enamino esters $ (X = NH0 O, S) are obtained in good to excellent yields by transamination reactions from ethyl 3-dimethylamino acrylate 2(a-e) and various volatile amines 3(a-e) using solvent-free conditions assisted by focused microwave irradiation. Most of the tz-hetero ~-enamino
A New Route to ฮฑ-Hetero ฮฒ-Enamino Esters Using a Mild and Convenient Solvent-Free Process Assisted by Focused Microwave Irradiation. -Neat microwave irradiation of a mixture of the ฮฑ