| Autor: |
Tomas Tejero, Francisco L. Merchan, Sonia Anoro, Pedro Merino |
| Jazyk: |
angličtina |
| Rok vydání: |
2000 |
| Předmět: |
|
| Zdroj: |
Molecules, Vol 5, Iss 2, Pp 132-152 (2000) |
| Druh dokumentu: |
article |
| ISSN: |
1420-3049 |
| DOI: |
10.3390/50200132 |
| Popis: |
The 1,3-dipolar cycloaddition reaction of N-benzyl-C-(2-furyl)nitrones with electron-rich alkenes gives preferentially trans-substituted 3,5-disubstituted isoxazolidines (endo approach). These experimental results are in good qualitative agreement with the predicted ones by semiempirical (AM1 and PM3) and ab initio (HF/3-21G) methods. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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