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 Citations (Scopus)

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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Alkenes
Esters

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

Regio- and diastereoselective synthesis of cyclic amino esters. / Park, Kyung Ho; Kurth, Thomas M.; Olmstead, Marilyn M.; Kurth, Mark J.

In: Tetrahedron Letters, Vol. 42, No. 6, 05.02.2001, p. 991-992.

Research output: Contribution to journalArticle

Park, KH, Kurth, TM, Olmstead, MM & Kurth, MJ 2001, 'Regio- and diastereoselective synthesis of cyclic amino esters', Tetrahedron Letters, vol. 42, no. 6, pp. 991-992. https://doi.org/10.1016/S0040-4039(00)02217-6
Park, Kyung Ho ; Kurth, Thomas M. ; Olmstead, Marilyn M. ; Kurth, Mark J. / Regio- and diastereoselective synthesis of cyclic amino esters. In: Tetrahedron Letters. 2001 ; Vol. 42, No. 6. pp. 991-992.
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