Enantioselective synthesis of the fully functionalized ABC ring of zoanthenol

Naoki Sugano; Yuuki Koizumi; Go Hirai; Hiroki Oguri; Shoji Kobayashi; Shuji Yamashita; Masahiro Hirama

doi:10.1002/asia.200800079

Enantioselective synthesis of the fully functionalized ABC ring of zoanthenol

Naoki Sugano, Yuuki Koizumi, Go Hirai, Hiroki Oguri, Shoji Kobayashi, Shuji Yamashita, Masahiro Hirama

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

14 被引用数 (Scopus)

抄録

Zoanthenol, isolated from Zoanthus sp., possesses an extremely complex architecture including contiguous quaternary carbons. An enantioselective synthesis of the fully functionalized ABC-ring of zoanthenol has been achieved and is described herein. The key features of the synthesis are the enzymatic kinetic optical resolution and the Mizoroki-Heck/Simmons-Smith reaction strategy used to construct the congested asymmetric quaternary carbons.

本文言語	英語
ページ（範囲）	1549-1557
ページ数	9
ジャーナル	Chemistry - An Asian Journal
巻	3
号	8-9
DOI	https://doi.org/10.1002/asia.200800079
出版ステータス	出版済み - 9月 1 2008
外部発表	はい

!!!All Science Journal Classification (ASJC) codes

生化学
有機化学

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10.1002/asia.200800079

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abstract = "Zoanthenol, isolated from Zoanthus sp., possesses an extremely complex architecture including contiguous quaternary carbons. An enantioselective synthesis of the fully functionalized ABC-ring of zoanthenol has been achieved and is described herein. The key features of the synthesis are the enzymatic kinetic optical resolution and the Mizoroki-Heck/Simmons-Smith reaction strategy used to construct the congested asymmetric quaternary carbons.",

author = "Naoki Sugano and Yuuki Koizumi and Go Hirai and Hiroki Oguri and Shoji Kobayashi and Shuji Yamashita and Masahiro Hirama",

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T1 - Enantioselective synthesis of the fully functionalized ABC ring of zoanthenol

AU - Sugano, Naoki

AU - Koizumi, Yuuki

AU - Hirai, Go

AU - Oguri, Hiroki

AU - Kobayashi, Shoji

AU - Yamashita, Shuji

AU - Hirama, Masahiro

PY - 2008/9/1

Y1 - 2008/9/1

N2 - Zoanthenol, isolated from Zoanthus sp., possesses an extremely complex architecture including contiguous quaternary carbons. An enantioselective synthesis of the fully functionalized ABC-ring of zoanthenol has been achieved and is described herein. The key features of the synthesis are the enzymatic kinetic optical resolution and the Mizoroki-Heck/Simmons-Smith reaction strategy used to construct the congested asymmetric quaternary carbons.

AB - Zoanthenol, isolated from Zoanthus sp., possesses an extremely complex architecture including contiguous quaternary carbons. An enantioselective synthesis of the fully functionalized ABC-ring of zoanthenol has been achieved and is described herein. The key features of the synthesis are the enzymatic kinetic optical resolution and the Mizoroki-Heck/Simmons-Smith reaction strategy used to construct the congested asymmetric quaternary carbons.

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JF - Chemistry - An Asian Journal

SN - 1861-4728

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Enantioselective synthesis of the fully functionalized ABC ring of zoanthenol

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!!!All Science Journal Classification (ASJC) codes

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