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Exo-Diastereoselective 1,3-dipolar cycloadditions of azomethine ylides to (2R)-3-Benzoyl-4-methylene-2-phenyloxazolidin-5-one

Journal Article


Abstract


  • Exo-diastereoselective 1,3-dipolar cycloadditions of azomethine ylides derived from α-amino ac acid esters to (2R)-3-Benzoyl-4-methylene-2-phenyloxazolidin-5-one (1) are reported. The cycloaddition products are conveniently converted to polyfunctional prolines in high enantiomeric purity. © 1995.

Publication Date


  • 1995

Citation


  • Pyne, S. G., Safaei-G., J., & Koller (in part), F. (1995). Exo-Diastereoselective 1,3-dipolar cycloadditions of azomethine ylides to (2R)-3-Benzoyl-4-methylene-2-phenyloxazolidin-5-one. Tetrahedron Letters, 36(14), 2511-2514. doi:10.1016/0040-4039(95)00294-M

Scopus Eid


  • 2-s2.0-0028909468

Web Of Science Accession Number


Start Page


  • 2511

End Page


  • 2514

Volume


  • 36

Issue


  • 14

Abstract


  • Exo-diastereoselective 1,3-dipolar cycloadditions of azomethine ylides derived from α-amino ac acid esters to (2R)-3-Benzoyl-4-methylene-2-phenyloxazolidin-5-one (1) are reported. The cycloaddition products are conveniently converted to polyfunctional prolines in high enantiomeric purity. © 1995.

Publication Date


  • 1995

Citation


  • Pyne, S. G., Safaei-G., J., & Koller (in part), F. (1995). Exo-Diastereoselective 1,3-dipolar cycloadditions of azomethine ylides to (2R)-3-Benzoyl-4-methylene-2-phenyloxazolidin-5-one. Tetrahedron Letters, 36(14), 2511-2514. doi:10.1016/0040-4039(95)00294-M

Scopus Eid


  • 2-s2.0-0028909468

Web Of Science Accession Number


Start Page


  • 2511

End Page


  • 2514

Volume


  • 36

Issue


  • 14