ChemInform Abstract: Enamide-Benzyne-[2 + 2] Cycloaddition: Stereoselective Tandem [2 + 2]—Pericyclic Ring-Opening—Intramolecular N-Tethered [4 + 2] Cycloadditions.
✍ Scribed by John B. Feltenberger; Ryuji Hayashi; Yu Tang; Eric S. C. Babiash; Richard P. Hsung
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 47 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
High-Pressure Promoted Stereoselective Tandem [4 + 2]/[3 + 2] Cycloadditions of Nitroalkenes and Enol Ethers. -The tandem cycloadditions of the nitroalkenes (I) and (V) with ethyl vinyl ether are found to be strongly accelerated under high pressure. The reactions proceed regioand stereoselectively.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v