Transannular Diels-Alder model studies on the total synthesis of chatancin. The furanophane approach. Part 2 [1]: Macrocyclization and Diels-Alder reaction
✍ Scribed by András Toró; Yuan Wang; Marc Drouin; Pierre Deslongchamps
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 231 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
Synthesis of three generations of model substrates with advancing similarity to chatancin are presented. In the first two generations, an Ireland-Ciaisen based six-step sequence supplied the trans-dienophile to be connected by dithiane chemistry to furfurals. In the third generation, a homogeraniol
Transannular Diels-Alder Model Studies on the Total Synthesis of Chatancin. The Furanophane Approach. Part 1. Assembly of the Acyclic Substrates. -In continuation of efforts on the total synthesis of the PAF antagonist chatancin (II), the synthesis of the open-chain compound (I) as substrate for a
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