Skip to main content
placeholder image

A New Strategy for the Diastereoselective Synthesis of Polyfunctionalized Pyrrolidines

Journal Article


Abstract


  • This paper describes a new strategy for the synthesis of polyfuncticnalized pyrrolidines via the ring-closing metathesis reaction of substituted 3-allyl-4-vinyl-2-oxazolindones and subsequent diastereoselective cis-dihydroxylation of the resulting pyrrolo[1,2-c]oxazol-3-ones.

Publication Date


  • 2004

Citation


  • Davis, A. S., Gates, N. J., Lindsay, K. B., Tang, M., & Pyne, S. G. (2004). A New Strategy for the Diastereoselective Synthesis of Polyfunctionalized Pyrrolidines. Synlett, (1), 49-52. doi:10.1055/s-2003-43362

Scopus Eid


  • 2-s2.0-0347601837

Web Of Science Accession Number


Start Page


  • 49

End Page


  • 52

Issue


  • 1

Abstract


  • This paper describes a new strategy for the synthesis of polyfuncticnalized pyrrolidines via the ring-closing metathesis reaction of substituted 3-allyl-4-vinyl-2-oxazolindones and subsequent diastereoselective cis-dihydroxylation of the resulting pyrrolo[1,2-c]oxazol-3-ones.

Publication Date


  • 2004

Citation


  • Davis, A. S., Gates, N. J., Lindsay, K. B., Tang, M., & Pyne, S. G. (2004). A New Strategy for the Diastereoselective Synthesis of Polyfunctionalized Pyrrolidines. Synlett, (1), 49-52. doi:10.1055/s-2003-43362

Scopus Eid


  • 2-s2.0-0347601837

Web Of Science Accession Number


Start Page


  • 49

End Page


  • 52

Issue


  • 1