Regio- and diastereoselective synthesis of cyclic amino esters

Kyung Ho Park, Thomas M. Kurth, Marilyn M. Olmstead, Mark J. Kurth

Research output: Contribution to journalArticle

10 Scopus citations

Abstract

Several cyclic amino esters have been prepared regio- and diastereoselectively depending on the electrophile (cis or trans alkene) and its leaving group.

Original languageEnglish (US)
Pages (from-to)991-992
Number of pages2
JournalTetrahedron Letters
Volume42
Issue number6
DOIs
StatePublished - Feb 5 2001

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ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Park, K. H., Kurth, T. M., Olmstead, M. M., & Kurth, M. J. (2001). Regio- and diastereoselective synthesis of cyclic amino esters. Tetrahedron Letters, 42(6), 991-992. https://doi.org/10.1016/S0040-4039(00)02217-6