Synthesis of (+)-Homononactic Acid via Iodoetherification

Hiromasa Kiyota, Masaki Abe, Yukie Ono, Takayuki Oritani

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

(+)-Homononactic acid, one of the monomers of polynactin, and its 8-epimer were synthesized. The key step was cis-selective iodoetherification of the enone or the α-silyloxyolefin intermediates constructed with Wittig-Horner or Julia coupling reactions, respectively.

Original languageEnglish
Pages (from-to)1093-1095
Number of pages3
JournalSynlett
Volume1997
Issue number9
Publication statusPublished - 1997
Externally publishedYes

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Monomers
Acids

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Kiyota, H., Abe, M., Ono, Y., & Oritani, T. (1997). Synthesis of (+)-Homononactic Acid via Iodoetherification. Synlett, 1997(9), 1093-1095.

Synthesis of (+)-Homononactic Acid via Iodoetherification. / Kiyota, Hiromasa; Abe, Masaki; Ono, Yukie; Oritani, Takayuki.

In: Synlett, Vol. 1997, No. 9, 1997, p. 1093-1095.

Research output: Contribution to journalArticle

Kiyota, H, Abe, M, Ono, Y & Oritani, T 1997, 'Synthesis of (+)-Homononactic Acid via Iodoetherification', Synlett, vol. 1997, no. 9, pp. 1093-1095.
Kiyota H, Abe M, Ono Y, Oritani T. Synthesis of (+)-Homononactic Acid via Iodoetherification. Synlett. 1997;1997(9):1093-1095.
Kiyota, Hiromasa ; Abe, Masaki ; Ono, Yukie ; Oritani, Takayuki. / Synthesis of (+)-Homononactic Acid via Iodoetherification. In: Synlett. 1997 ; Vol. 1997, No. 9. pp. 1093-1095.
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