New Lead Structures by Diels-Alder Reactions of Streptazolin with Naphthoquinones
✍ Scribed by Dr. Susanne Grabley; Dr. Heinz Kluge; Dr. Hans-Ullrich Hoppe
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 240 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Soluble propeller-like polyarylates with &fn 2 1 x 104 and melting in the range 200-220°C were synthesized via one-pot simultaneous Diels-Alder (using anthracene or (E,E)-I ,4-diphenylbutadiene as enophile and the fumaroyl moiety as dienophile) and polycondensation reaction. Thermal properties of al
The first reported cycloaddition reactions of 2-styryl-bromination/dehydrobromination processes. These benzoflavone derivatives were also obtained in one-pot chromones with ortho-benzoquinodimethane afforded 2-[2-(3-aryl-1,2,3,4-tetrahydronaphthyl)]chromones. These cyclo-cycloaddition reactions of 2
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