The Synthesis of Pentacyclo[7.3.1.14,12.02,7.06,11]tetradecane
β Scribed by P. v. R. Schleyer
- Publisher
- John Wiley and Sons
- Year
- 1965
- Tongue
- English
- Weight
- 287 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0044-8249
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π SIMILAR VOLUMES
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
Cm irradiation, cyclopentadiene dimer (3 and its enone derivatives (L,s$ are converted easily to the corresponding cage compounds, 5, 16\* 73and84 .." ,' u \_, by intramolecular cycloaddition, whereas the corresponding transformation of a six-membered analog, from cyclohexadiene dimer (9\_) to lO\_,
Ptrgamon Press. Prlnttd III Great Brltarn. FLASH THERMOLYSIS OF 3,7-DIISOPROPYLIDENETETRACYCLO [3.3.1.02"+.06'8] NONANE. AN ACCESS TO THE PENTACYCLO [4.3.0.02'~,03~\*.057JN0N~NE SYSTEM