Double diastereoselectivity in the intramolecular nitrile oxide-olefin cycloaddition (INOC) reaction.

Hyoung Rae Kim, Hyung Jin Kim, Jetty L. Duffy, Marilyn M. Olmstead, Karin Ruhlandt, Mark J. Kurth

Research output: Contribution to journalArticle

35 Citations (Scopus)

Abstract

An investigation of relative asymmetric induction and double diastereoselectivity in the intramolecular nitrile oxide-olefin cycloaddition (INOC) reaction is presented.

Original languageEnglish (US)
Pages (from-to)4259-4262
Number of pages4
JournalTetrahedron Letters
Volume32
Issue number34
DOIs
StatePublished - 1991
Externally publishedYes

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Nitriles
Cycloaddition
Cycloaddition Reaction
Alkenes
Oxides

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Double diastereoselectivity in the intramolecular nitrile oxide-olefin cycloaddition (INOC) reaction. / Rae Kim, Hyoung; Jin Kim, Hyung; Duffy, Jetty L.; Olmstead, Marilyn M.; Ruhlandt, Karin; Kurth, Mark J.

In: Tetrahedron Letters, Vol. 32, No. 34, 1991, p. 4259-4262.

Research output: Contribution to journalArticle

Rae Kim, Hyoung ; Jin Kim, Hyung ; Duffy, Jetty L. ; Olmstead, Marilyn M. ; Ruhlandt, Karin ; Kurth, Mark J. / Double diastereoselectivity in the intramolecular nitrile oxide-olefin cycloaddition (INOC) reaction. In: Tetrahedron Letters. 1991 ; Vol. 32, No. 34. pp. 4259-4262.
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AU - Ruhlandt, Karin

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