Synthesis of the H ring of gambierol

Isao Kadota, Akio Ohno, Yasuhisa Matsukawa, Yoshinori Yamamoto

Research output: Contribution to journalArticle

58 Citations (Scopus)

Abstract

Stereoselective synthesis of the H ring of gambierol was achieved from 2-deoxy-D-ribose by using the intramolecular reaction of allylstannane with aldehyde as a key step. Modified Stille coupling was successfully applied for the construction of the triene side chain.

Original languageEnglish
Pages (from-to)6373-6376
Number of pages4
JournalTetrahedron Letters
Volume39
Issue number35
DOIs
Publication statusPublished - Aug 27 1998
Externally publishedYes

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Ribose
Aldehydes
gambierol

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Synthesis of the H ring of gambierol. / Kadota, Isao; Ohno, Akio; Matsukawa, Yasuhisa; Yamamoto, Yoshinori.

In: Tetrahedron Letters, Vol. 39, No. 35, 27.08.1998, p. 6373-6376.

Research output: Contribution to journalArticle

Kadota, I, Ohno, A, Matsukawa, Y & Yamamoto, Y 1998, 'Synthesis of the H ring of gambierol', Tetrahedron Letters, vol. 39, no. 35, pp. 6373-6376. https://doi.org/10.1016/S0040-4039(98)01312-4
Kadota, Isao ; Ohno, Akio ; Matsukawa, Yasuhisa ; Yamamoto, Yoshinori. / Synthesis of the H ring of gambierol. In: Tetrahedron Letters. 1998 ; Vol. 39, No. 35. pp. 6373-6376.
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