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

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

Digital Object Identifier (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.

UOW Authors

•   Pyne, Stephen

Publication Date

• 1995

Publisher

• Elsevier BV 

Published In

• Tetrahedron Letters  Journal

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

Digital Object Identifier (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