A new method for constructing 5,6,11,12-tetradehydrodibenzo[a,e]cyclooctene is described on the basis of one-pot double elimination protocol. The target molecule, which is the smallest cyclophane with alternate arylene-ethynylene linkage, is synthesized in 61 % yield through oxidative dimerization o
β¦ LIBER β¦
Synthesis and reactions of 5,6,11,12-tetradehydrodibenzo[a,e]cyclooctene and 5,6-didehydrodibenzo[a,e]cyclooctene
β Scribed by Henry N.C. Wong; Franz Sondheimer
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 991 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4020
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