## Abstract The title compounds have been isolated and their structures determined by X‐ray crystallography. Their relative stability is discussed in terms of theory and experiment. The __endo__‐adduct is the thermodynamically more stable one.
Propellanes. LXVII. Reactions of 1, 6-bridged [10]annulenes with 4-methyl-1,2,4-triazoline-3, 5-dione
✍ Scribed by Pnina Ashkenazi; Emanuel Vogel; David Ginsburg
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- German
- Weight
- 287 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Reactions of 11‐substituted‐1, 6‐methano [10]annulenes and 1, 6‐methano [10]‐annulenes substituted in the aromatic ring with the title dienophile are described.
📜 SIMILAR VOLUMES
## Abstract Relatively few __exo__‐adducts have been obtained from the title compounds. Only one such mono‐adduct, **3**, is known. Several __exo‐endo__‐bis‐adducts have been obtained but the structure of one of these, **5**, has been proved unequivocally by X‐ray structural determination.
## Abstract Two isomeric propellane epoxides **1a** and **1b** containing a cyclohexadiene ring are attacked by the title dienophile as predicted, __syn__ to the five‐membered ether ring whose α‐hydrogens exert less repulsion than the α‐epoxy hydrogens or the epoxide oxygen, respectively, of the cy
## Abstract The title dienophiles attack nopadiene from the less hindered side.