An enantiocontrolled total synthesis of (-)-xanthorrhizol

Kenji Sato; Toshikazu Bando; Mitsuru Shindo; Kozo Shishido

doi:10.3987/com-98-s(h)4

An enantiocontrolled total synthesis of (-)-xanthorrhizol

Kenji Sato, Toshikazu Bando, Mitsuru Shindo, Kozo Shishido

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

11 被引用数 (Scopus)

抄録

An efficient and enantiocontrolled total synthesis of natural (-)- xanthorrhizol (3) has been accomplished by employing the lipase-mediated asymmetric acetylation of the σ-symmetrical prochiral 2-aryl-1,3-propanediol (7) leading to the formation of the optically enriched monoacetate (6) as the key step.

本文言語	英語
ページ（範囲）	11-15
ページ数	5
ジャーナル	Heterocycles
巻	50
号	1
DOI	https://doi.org/10.3987/com-98-s(h)4
出版ステータス	出版済み - 1月 1 1999
外部発表	はい

!!!All Science Journal Classification (ASJC) codes

分析化学
薬理学
有機化学

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10.3987/com-98-s(h)4

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abstract = "An efficient and enantiocontrolled total synthesis of natural (-)- xanthorrhizol (3) has been accomplished by employing the lipase-mediated asymmetric acetylation of the σ-symmetrical prochiral 2-aryl-1,3-propanediol (7) leading to the formation of the optically enriched monoacetate (6) as the key step.",

author = "Kenji Sato and Toshikazu Bando and Mitsuru Shindo and Kozo Shishido",

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AB - An efficient and enantiocontrolled total synthesis of natural (-)- xanthorrhizol (3) has been accomplished by employing the lipase-mediated asymmetric acetylation of the σ-symmetrical prochiral 2-aryl-1,3-propanediol (7) leading to the formation of the optically enriched monoacetate (6) as the key step.

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An enantiocontrolled total synthesis of (-)-xanthorrhizol

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!!!All Science Journal Classification (ASJC) codes

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