The cycloaddition of diphenylnitrilimine with coumarin and chromone gave the cycloadducts 4 and 5 respectively. The structures of these products were based on elemental and spectral analyses and alternate synthesis. The orientations of the cycloaddition are interpreted in terms of FM0 theory.
Regioselectivity and specificity in cycloaddition of diphenylnitrilimine
✍ Scribed by Saïd Kitane; Tshiamala Kabula; Joël Vebrel; Bernard Laude
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 142 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
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