A transannular diels-alder strategy to the construction of the CDE ring system of nakiterpiosin

Hiroyoshi Takamura, Yuji Yamagami, Tomonori Ito, Masahiro Ito, Hirokazu Arimoto, Isao Kadota, Daisuke Uemurat

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

The transannular Diels-Alder (TADA) reaction was applied to the synthesis of the CDE ring system of nakiterpiosin (1). TADA product 28 is a key intermediate toward the total synthesis of 1.

Original languageEnglish
Pages (from-to)351-364
Number of pages14
JournalHeterocycles
Volume77
Issue number1
DOIs
Publication statusPublished - Jan 1 2009

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Alnus
Cycloaddition Reaction
nakiterpiosin

Keywords

  • Marine Natural Product
  • Nakiterpiosin
  • Stille Coupling
  • Synthetic Study
  • Transannular Diels-Alder Reaction

ASJC Scopus subject areas

  • Analytical Chemistry
  • Organic Chemistry
  • Pharmacology

Cite this

A transannular diels-alder strategy to the construction of the CDE ring system of nakiterpiosin. / Takamura, Hiroyoshi; Yamagami, Yuji; Ito, Tomonori; Ito, Masahiro; Arimoto, Hirokazu; Kadota, Isao; Uemurat, Daisuke.

In: Heterocycles, Vol. 77, No. 1, 01.01.2009, p. 351-364.

Research output: Contribution to journalArticle

Takamura, Hiroyoshi ; Yamagami, Yuji ; Ito, Tomonori ; Ito, Masahiro ; Arimoto, Hirokazu ; Kadota, Isao ; Uemurat, Daisuke. / A transannular diels-alder strategy to the construction of the CDE ring system of nakiterpiosin. In: Heterocycles. 2009 ; Vol. 77, No. 1. pp. 351-364.
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