Total synthesis of (-)-Pramanicin

Shin ya Aoki; Taro Tsukude; Yukari Miyazaki; Ken ichi Takao; Kin ichi Tadano

doi:10.3987/com-06-s(o)5

Total synthesis of (-)-Pramanicin

Shin ya Aoki, Taro Tsukude, Yukari Miyazaki, Ken ichi Takao, Kin ichi Tadano

応用化学科

研究成果: Article › 査読

11 被引用数 (Scopus)

抄録

The total synthesis of natural (-)-pramanicin, a highly oxygenated γlactam-type antifungal agent, is described. The enantiospecific total synthesis of this natural product commenced with 5-deoxy-1,2-O-isopropylidene-α-d-xylofuranose as an enantiopure starting material.

本文言語	English
ページ（範囲）	49-54
ページ数	6
ジャーナル	Heterocycles
巻	69
号	1
DOI	https://doi.org/10.3987/com-06-s(o)5
出版ステータス	Published - 2006 12月 1

ASJC Scopus subject areas

分析化学
薬理学
有機化学

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10.3987/com-06-s(o)5

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引用スタイル

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abstract = "The total synthesis of natural (-)-pramanicin, a highly oxygenated γlactam-type antifungal agent, is described. The enantiospecific total synthesis of this natural product commenced with 5-deoxy-1,2-O-isopropylidene-α-d-xylofuranose as an enantiopure starting material.",

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AU - Takao, Ken ichi

AU - Tadano, Kin ichi

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Y1 - 2006/12/1

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AB - The total synthesis of natural (-)-pramanicin, a highly oxygenated γlactam-type antifungal agent, is described. The enantiospecific total synthesis of this natural product commenced with 5-deoxy-1,2-O-isopropylidene-α-d-xylofuranose as an enantiopure starting material.

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Total synthesis of (-)-Pramanicin

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