The Clenanensen reduction of pentacyclo[6.4.0.02~7.03,11.06~10], dodecane-9,12-dione unexpectedly led to the formation of pentacyclo[6.4.0. 02.6.05,9.04.12]-2-dodecanol and pentacyclo[6.4.0.02~7.03,11.06,10]dodecane-1,Gdiol as main products. Tetracyclo[6.4.0.05,9.04,12]dodecane-2,7dione and its corr
β¦ LIBER β¦
The synthesis of pentacyclo[6.4.0.02,7.03,12.06,9]dodeca-4,10-diene a pentacyclic dimer of benzene
β Scribed by Nien-chu C. Yang; M.Glenn Horner
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 199 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
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