1,3-dipolar cycloadditions of n-benzyl furfuryl nitrones with electron-rich alkenes
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ID: 224927
2000
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Abstract
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.
| Reference Key |
tejero2000molecules1,3-dipolar
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|---|---|
| Authors | ;Tomas Tejero;Francisco L. Merchan;Sonia Anoro;Pedro Merino |
| Journal | Journal of ethnopharmacology |
| Year | 2000 |
| DOI |
10.3390/50200132
|
| URL | |
| Keywords | Keywords not found |
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