Facile retro diels-alder reaction of a vinyl lithium compound
✍ Scribed by Harold Hart; Khalil Shahlai
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 144 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Attempts to generate benzobarrelyne 8 by loss of lithium chloride from 4 resulted in a facile retro Diels-Alder reaction of the "dimeric" adduct formed by addition of 4 to 8.
📜 SIMILAR VOLUMES
## 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, please click on HTML or PDF.
## Abstract Under microwave conditions, o‐quinol dimers smoothly react with several olefins and acetylenes to afford bicyclooctenes with high diastereoselectivity.
## Abstract For Abstract see ChemInform Abstract in Full Text.