Model Reactions for Biological Ring Opening of Anthraquinones
β Scribed by Prof. Dr. B. Franck; Dipl.-Chem. V. Radtke; Dipl.-Chem. U. Zeidler
- Publisher
- John Wiley and Sons
- Year
- 1967
- Tongue
- English
- Weight
- 228 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The addition reaction of spiro orthoesters (SOEs) with electrophiles accompanying ring-opening isomerization was investigated as a model reaction for polyaddition of bifunctional SOEs with bifunctional electrophiles. Among several electrophiles such as carboxylic acids and carboxylic anhydrides, aci
The development of catalysts that are not only enantioselective and high yielding but also useful from a practical standpoint persists as a challenging goal in asymmetric synthesis. In the ideal case, a catalyst should be readily available or easily synthesized on any scale and should display both h