Absolute stereochemistry and synthesis of aplyronines B and C, the congeners of aplyronine A, a potent antitumor substance of marine origin

Kiyotake Suenaga, Takeshi Ishigaki, Akira Sakakura, Hideo Kigoshi, Kiyoyuki Yamada

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

Synthesis of aplyronines B and C, the congeners of aplyronine A, was achieved enantioselectively, which established their stereostructures.

Original languageEnglish
Pages (from-to)5053-5056
Number of pages4
JournalTetrahedron Letters
Volume36
Issue number28
DOIs
Publication statusPublished - 1995 Jul 10
Externally publishedYes

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Stereochemistry
aplyronine A
aplyronine C

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Absolute stereochemistry and synthesis of aplyronines B and C, the congeners of aplyronine A, a potent antitumor substance of marine origin. / Suenaga, Kiyotake; Ishigaki, Takeshi; Sakakura, Akira; Kigoshi, Hideo; Yamada, Kiyoyuki.

In: Tetrahedron Letters, Vol. 36, No. 28, 10.07.1995, p. 5053-5056.

Research output: Contribution to journalArticle

Suenaga, Kiyotake ; Ishigaki, Takeshi ; Sakakura, Akira ; Kigoshi, Hideo ; Yamada, Kiyoyuki. / Absolute stereochemistry and synthesis of aplyronines B and C, the congeners of aplyronine A, a potent antitumor substance of marine origin. In: Tetrahedron Letters. 1995 ; Vol. 36, No. 28. pp. 5053-5056.
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