Molecular orbital calculations were performed to examine the electronic effects involved in the regioselectivity in the 1,3-dipolar cycloaddition reaction of nitrone and fulminic acid. The substituted ethylene dipolarophiles were selected to represent a range of electron-donatingrwithdrawing abiliti
β¦ LIBER β¦
1,3-Dipolar Cycloadditions of Fulminic Acid
β Scribed by Prof. R. Huisgen; Dipl.-Chem. M. Christl
- Publisher
- John Wiley and Sons
- Year
- 1967
- Tongue
- English
- Weight
- 218 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0044-8249
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