Synthesis of 1,2-five-ring-annellated barrelenes via the intramolecular Diels-Alder reaction of acetylenic derivatives
✍ Scribed by Latchezar S. Trifonov; Alexander S. Orahovats
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- German
- Weight
- 321 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0018-019X
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📜 SIMILAR VOLUMES
A novel, efficient synthesis of a series of functionalized, benzo-annelated decahydrofuro [3,2h][1,6]naphthyridine derivatives 3 has been achieved. The protocol is based on the intramolecular hetero-Diels-Alder (IMHDA) reaction of in situ formed imines derived from an N-prenylated sugar aldehyde 1 a
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