Asymmetric synthesis of β-amino cyclic ethers via the intramolecular reaction of γ-alkoxyallylstannane with chiral imine

Jung Youl Park, Choul Hong Park, Isao Kadota, Yoshinori Yamamoto

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

The Lewis acid mediated cyclization of γ-oxygen substituted allylic stannane 1, having a chiral imine group at the terminus of the carbon chain, afforded trans-β-amino cyclic ether 2 with very high to good diastereoselectivities in high chemical yields.

Original languageEnglish
Pages (from-to)1791-1794
Number of pages4
JournalTetrahedron Letters
Volume39
Issue number13
DOIs
Publication statusPublished - Mar 26 1998
Externally publishedYes

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Cyclic Ethers
Lewis Acids
Imines
Cyclization
Carbon
Oxygen
stannane

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Asymmetric synthesis of β-amino cyclic ethers via the intramolecular reaction of γ-alkoxyallylstannane with chiral imine. / Park, Jung Youl; Park, Choul Hong; Kadota, Isao; Yamamoto, Yoshinori.

In: Tetrahedron Letters, Vol. 39, No. 13, 26.03.1998, p. 1791-1794.

Research output: Contribution to journalArticle

Park, Jung Youl ; Park, Choul Hong ; Kadota, Isao ; Yamamoto, Yoshinori. / Asymmetric synthesis of β-amino cyclic ethers via the intramolecular reaction of γ-alkoxyallylstannane with chiral imine. In: Tetrahedron Letters. 1998 ; Vol. 39, No. 13. pp. 1791-1794.
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