Synthesis of (+)-Homononactic Acid via Iodoetherification

Hiromasa Kiyota; Masaki Abe; Yukie Ono; Takayuki Oritani

doi:10.1055/s-1997-1547

Synthesis of (+)-Homononactic Acid via Iodoetherification

Hiromasa Kiyota, Masaki Abe, Yukie Ono, Takayuki Oritani

研究成果 › 査読

18 被引用数 (Scopus)

抄録

(+)-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.

本文言語	English
ページ（範囲）	1093-1095
ページ数	3
ジャーナル	Synlett
巻	1997
号	9
DOI	https://doi.org/10.1055/s-1997-1547
出版ステータス	Published - 1月 1 1997
外部発表	はい

ASJC Scopus subject areas

有機化学

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10.1055/s-1997-1547

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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.",

author = "Hiromasa Kiyota and Masaki Abe and Yukie Ono and Takayuki Oritani",

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AU - Oritani, Takayuki

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Y1 - 1997/1/1

N2 - (+)-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.

AB - (+)-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.

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Synthesis of (+)-Homononactic Acid via Iodoetherification

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