The thermal decarbonylation of the 3-cyclopentenone system to the butadiene system has been discussed theoretically (eq. 1). 1 Furthermore, the surprising ease of the thermal decarbonylation of the norbornen-7-one system producinq cyclohexadiene is also well documented (eq. 2).' Recently, we succes
Steric acceleration in the thermal decarbonylation of highly compressed norbornen-7-ones
✍ Scribed by R. McCulloch; A.R. Rye; D. Wege
- Publisher
- Elsevier Science
- Year
- 1969
- Tongue
- French
- Weight
- 225 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Norbornadien-'I-one 2 and its benzo-annellated derivatives are highly reactive molecules, which readily undergo thermal deoarbonylution to yield benzene and its benzo-annellated derivatives.1 Although the factors which contribute to the high reactivity of 4 and its derivatives have not been fully determined, they are apparently largely electronic in nature?
Norbornen-7-one 4 substituted nor~ornen-7-ones undergo thermal decarbonylation with varying ease. Thus locten-l-one is reactive, looeee monoxide give at while exo-trioyc10[3.2.1.
📜 SIMILAR VOLUMES
## Abstract Acid treatment of 9__exo__‐methyl‐__anti__^10,11^‐tricyclo[4.2.1.1^2,5^]deca‐3,7‐diene‐9__endo__, 10__endo__‐diol (**8**) leads to the two isomeric pentacyclic ethers **7** and **9** by intramolecular nucleophilic substitution of a protonated OH‐group with participation of a C,C‐double