Stereoselective synthesis of the chiral tetrahydropyrane core of swinholides and misakinolides

Hiroyuki Hayakawa; Kouki Iida; Masahiro Miyazawa; Masaaki Miyashita

doi:10.1246/cl.1999.601

Stereoselective synthesis of the chiral tetrahydropyrane core of swinholides and misakinolides

Hiroyuki Hayakawa, Kouki Iida, Masahiro Miyazawa, Masaaki Miyashita^*

^*この論文の責任著者

化学科

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

7 被引用数 (Scopus)

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Stereoselective synthesis of the optically pure tetrahydropyrane core of swinholides and misakinolide A starting from (S)-methyl lactate is described in which the highly stereoselective intramolecular iodoetherification for construction of the tetrahydropyrane ring and the regioselective ring-opening reaction of an epoxide are involved as key steps.

本文言語	英語
ページ（範囲）	601-602
ページ数	2
ジャーナル	Chemistry Letters
号	7
DOI	https://doi.org/10.1246/cl.1999.601
出版ステータス	出版済み - 1999

ASJC Scopus 主題領域

化学一般

文献へのアクセス

10.1246/cl.1999.601

引用スタイル

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title = "Stereoselective synthesis of the chiral tetrahydropyrane core of swinholides and misakinolides",

abstract = "Stereoselective synthesis of the optically pure tetrahydropyrane core of swinholides and misakinolide A starting from (S)-methyl lactate is described in which the highly stereoselective intramolecular iodoetherification for construction of the tetrahydropyrane ring and the regioselective ring-opening reaction of an epoxide are involved as key steps.",

author = "Hiroyuki Hayakawa and Kouki Iida and Masahiro Miyazawa and Masaaki Miyashita",

year = "1999",

doi = "10.1246/cl.1999.601",

language = "英語",

pages = "601--602",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "Oxford University Press",

number = "7",

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T1 - Stereoselective synthesis of the chiral tetrahydropyrane core of swinholides and misakinolides

AU - Hayakawa, Hiroyuki

AU - Iida, Kouki

AU - Miyazawa, Masahiro

AU - Miyashita, Masaaki

PY - 1999

Y1 - 1999

N2 - Stereoselective synthesis of the optically pure tetrahydropyrane core of swinholides and misakinolide A starting from (S)-methyl lactate is described in which the highly stereoselective intramolecular iodoetherification for construction of the tetrahydropyrane ring and the regioselective ring-opening reaction of an epoxide are involved as key steps.

AB - Stereoselective synthesis of the optically pure tetrahydropyrane core of swinholides and misakinolide A starting from (S)-methyl lactate is described in which the highly stereoselective intramolecular iodoetherification for construction of the tetrahydropyrane ring and the regioselective ring-opening reaction of an epoxide are involved as key steps.

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U2 - 10.1246/cl.1999.601

DO - 10.1246/cl.1999.601

M3 - 学術論文

AN - SCOPUS:0033245476

SN - 0366-7022

SP - 601

EP - 602

JO - Chemistry Letters

JF - Chemistry Letters

IS - 7

ER -

Stereoselective synthesis of the chiral tetrahydropyrane core of swinholides and misakinolides

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