Lactols in stereoselection 2. Stereoselective synthesis of disubstituted cyclic ethers.

Katsuhiko Tomooka, Kenji Matsuzawa, Keisuke Suzuki, Gen ichi Tsuchihashi

Research output: Contribution to journalArticle

56 Citations (Scopus)

Abstract

Direct reaction of lactols with organometals (Met. = Al, Ti, Zn, Sn) in the presence of Lewis acid provides disubstituted tetrahydrofurans and tetrahydropyrans with high diastereoselectivity.

Original languageEnglish
Pages (from-to)6339-6342
Number of pages4
JournalTetrahedron Letters
Volume28
Issue number50
DOIs
Publication statusPublished - Jan 1 1987

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Cyclic Ethers
Furans
Lewis Acids

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

Lactols in stereoselection 2. Stereoselective synthesis of disubstituted cyclic ethers. / Tomooka, Katsuhiko; Matsuzawa, Kenji; Suzuki, Keisuke; Tsuchihashi, Gen ichi.

In: Tetrahedron Letters, Vol. 28, No. 50, 01.01.1987, p. 6339-6342.

Research output: Contribution to journalArticle

Tomooka, Katsuhiko ; Matsuzawa, Kenji ; Suzuki, Keisuke ; Tsuchihashi, Gen ichi. / Lactols in stereoselection 2. Stereoselective synthesis of disubstituted cyclic ethers. In: Tetrahedron Letters. 1987 ; Vol. 28, No. 50. pp. 6339-6342.
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