1,3-Dipolar Cycloadditions of N-Benzyl Furfuryl Nitrones with Electron-rich Alkenes

1,3-Dipolar Cycloadditions of N-Benzyl Furfuryl Nitrones with Electron-rich Alkenes

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 PM...

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Bibliographic Details
Main Authors: Tomas Tejero, Francisco L. Merchan, Sonia Anoro, Pedro Merino
Format: Article
Language:English
Published: MDPI AG 2000-02-01
Series:Molecules
Subjects:
Nitrones
isoxazolidines
pyrrolidines
theoretical calculations
cycloaddition
Online Access:http://www.mdpi.com/1420-3049/5/2/132/

Internet

http://www.mdpi.com/1420-3049/5/2/132/

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