Stereochemical aspects of the intramolecular Diels-Alder reactions of methyl (E,E,E)- and (Z,E,E)-6-alkoxy-11-methyldodeca-2,7,9-trienoate
✍ Scribed by Roush, William R.
- Book ID
- 127262446
- Publisher
- American Chemical Society
- Year
- 1979
- Tongue
- English
- Weight
- 430 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Abstract4 A mixture of tetrachiral deca-1,7E,9-triene 2 and its 72 isomer 2 was prepared from D-glucose by the use of two Wittig olefination reactions. When 5 or 6 were subjected to intramolecular Diels-Alder reaction un'-er Thermal conditions the same, cis-fused octahydronaphtalene enantiomer 9 was
An efficient catalytic double asymmetric induction during the tandem transetherification-intramolecular hetero Diels-Alder reaction has been developed. The enantioselective tandem reaction of methyl (E)-4-methoxy-2-oxo-3-butenoate with rac-6-methyl-5-hepten-2-ol has been achieved to provide methyl (