Total synthesis of methyl sarcophytoate

Takahiro Ichige, Yusuke Okano, Naoki Kanoh, Masaya Nakata

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Together with the improved synthesis of the diene unit 15 of methyl sarcophytoate (1), a biscembranoid marine natural product, the asymmetric total synthesis of 1 was achieved by the thermal Diels-Alder reaction between the dienophile unit, methyl sarcoate (2), and 15.

Original languageEnglish
Pages (from-to)9862-9863
Number of pages2
JournalJournal of the American Chemical Society
Volume129
Issue number32
DOIs
Publication statusPublished - 2007 Aug 15

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Cycloaddition Reaction
Biological Products
Hot Temperature
methyl sarcophytoate

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Ichige, T., Okano, Y., Kanoh, N., & Nakata, M. (2007). Total synthesis of methyl sarcophytoate. Journal of the American Chemical Society, 129(32), 9862-9863. https://doi.org/10.1021/ja073952e

Total synthesis of methyl sarcophytoate. / Ichige, Takahiro; Okano, Yusuke; Kanoh, Naoki; Nakata, Masaya.

In: Journal of the American Chemical Society, Vol. 129, No. 32, 15.08.2007, p. 9862-9863.

Research output: Contribution to journalArticle

Ichige, T, Okano, Y, Kanoh, N & Nakata, M 2007, 'Total synthesis of methyl sarcophytoate', Journal of the American Chemical Society, vol. 129, no. 32, pp. 9862-9863. https://doi.org/10.1021/ja073952e
Ichige, Takahiro ; Okano, Yusuke ; Kanoh, Naoki ; Nakata, Masaya. / Total synthesis of methyl sarcophytoate. In: Journal of the American Chemical Society. 2007 ; Vol. 129, No. 32. pp. 9862-9863.
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