Cycloaddition and polymerization reactions of N-ethyl-3-vinylcarbazole with electron-poor olefins
β Scribed by Abdelkader, M.; Hall, H. K.
- Book ID
- 126895290
- Publisher
- American Chemical Society
- Year
- 1982
- Tongue
- English
- Weight
- 563 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## 3-Diazo-4-methyl-5-phenylpyrazole readily adds to electron rich olefins to give 1,7-cycloadducts, The mechanism of the reaction consists of an initial 1,3-dipolar cycloaddition followed by a subsequent rearrangement.
Summmy. 1-Thia-3-azabutadienes cleanly undergo [4 + 21 cycloaddition processes with electron-poor dienophiles; the reaction is regioselective and leads exclusively to the endo isomer.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v