## Abstract Thermolyses of the title compounds at various temperatures have been investigated. At the lower end of the temperature range studied indazoles **5a**, **b** are formed in nearly quantitative yields, while at the upper end formal carbene‐type reaction‐products **6**, **7**, **8** have be
✦ LIBER ✦
Acetolysis of 4-endo-diazoacetyl-bicyclo[3.1.0]hexene: a new synthesis of semibullvalene. Preliminary communication
✍ Scribed by Roger Malherbe
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- German
- Weight
- 132 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Acetolysis of diazoketone 1 gives in good yield 6‐acetoxy‐tricyclo[3.3.0.0^2,8^]octan‐3‐one (2) which is converted into semibullvalene in a three‐step sequence. Compound 2 is potentially a good starting material for 3,6‐substituted semibullvalenes.
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