Inverse electron demand Diels-Alder reactions of indole V. Reactions of 3-substituted indoles with heteroaromatic azadienes
β Scribed by Scott C. Benson; Lily Lee; John K. Snyder
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- French
- Weight
- 257 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Benzamidine (I) reacts with several s-tetrazines to give as-triazines in moderate to good yield, together with some s-triazines; separate experiments have shown that these are due to the fact that (I) also undergoes Diels-Alderreactions with as-and even with s-triazines. Although the so-called "Diel
Ultrasound irradiaton accelerates hetero Diels-Alder reactions between l-dimethylamino-I-azadienes and electron-defficient dienophiles. Besides the lower reaction times and increased yields, other advantages of the sonicated reactions are the possibility of isolating previously unknown adducts due t