Total synthesis of (±)-5-deoxystrigol via reductive carbon-carbon bond formation

Mitsuru Shoji, Eriko Suzuki, Minoru Ueda

Research output: Contribution to journal › Article

12 Citations (Scopus)

Abstract

(Chemical Equation Presented) The total synthesis of 5-deoxystrigol was successfully carried out via the regioselective coupling reaction between the aluminum ate complex of an alkyne and an epoxide and the two reductive carbon-carbon bond formations in the presence of transition metals as key steps.

Original languageEnglish
Pages (from-to)3966-3969
Number of pages4
JournalJournal of Organic Chemistry
Volume74
Issue number10
DOIs
Publication statusPublished - 2009 May 15
Externally publishedYes

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Carbon
Alkynes
Epoxy Compounds
Aluminum
Transition metals
Metals
5-deoxystrigol

ASJC Scopus subject areas

  • Organic Chemistry
  • Medicine(all)

Cite this

Total synthesis of (±)-5-deoxystrigol via reductive carbon-carbon bond formation. / Shoji, Mitsuru; Suzuki, Eriko; Ueda, Minoru.

In: Journal of Organic Chemistry, Vol. 74, No. 10, 15.05.2009, p. 3966-3969.

Research output: Contribution to journal › Article

Shoji, M, Suzuki, E & Ueda, M 2009, 'Total synthesis of (±)-5-deoxystrigol via reductive carbon-carbon bond formation', Journal of Organic Chemistry, vol. 74, no. 10, pp. 3966-3969. https://doi.org/10.1021/jo9002085
Shoji M, Suzuki E, Ueda M. Total synthesis of (±)-5-deoxystrigol via reductive carbon-carbon bond formation. Journal of Organic Chemistry. 2009 May 15;74(10):3966-3969. https://doi.org/10.1021/jo9002085
Shoji, Mitsuru ; Suzuki, Eriko ; Ueda, Minoru. / Total synthesis of (±)-5-deoxystrigol via reductive carbon-carbon bond formation. In: Journal of Organic Chemistry. 2009 ; Vol. 74, No. 10. pp. 3966-3969.
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