**2‐Thia‐7‐aza‐isotwistanes**. The access to the 2‐thia‐7‐aza‐isotwistane system was achieved by water addition to the twistene **1** yielding the isotwistanol **2**, characterized also as its acetate **4**. Analogous D~2~O/D~2~SO~4~‐treatment of the twistene **1** (→ **3**) allowed to deduce the r
Heterotricyclodecane XXII 2-Aza-7-thia-isotwistane
✍ Scribed by Henry Szczepanski; Camille Ganter
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- German
- Weight
- 616 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
2‐Aza‐7‐thia‐isotwistanes.
2‐Aza‐7‐thia‐isotwistanes were synthesized either starting from suitable 9‐thiabicyclo[3.3.1]nonenes by olefin‐amination (1 → 4, 2 → 5, 3 → 6, 8 → 10 and 9 → 11) as well as by intramolecular substitution (25 → 26) or by molecular rearrangement starting from twistanes (21 → 19 and 22 → 10). From the isotwistanes thus obtained several other compounds (7, 12–18, 20, 23 and 24) were prepared, too.
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