Expeditious and stereoselective synthesis of chiral trans -β-hydroxy-δ-lactone systems

Masahiro Miyazawa; Erika Matsuoka; Shinobu Sasaki; Satoshi Oonuma; Kimiyuki Maruyama; Masaaki Miyashita

doi:10.1246/cl.1998.109

Expeditious and stereoselective synthesis of chiral trans -β-hydroxy-δ-lactone systems

Masahiro Miyazawa, Erika Matsuoka, Shinobu Sasaki, Satoshi Oonuma, Kimiyuki Maruyama, 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

15 被引用数 (Scopus)

抄録

Expeditious and stereoselective synthesis of chiral trans-β-hydroxy-δ-lactone systems starting from γ,δ-epoxy acrylates is described which involves the regioselective ring opening of an epoxide and the intramolecular conjugate addition of a hemiacetal alkoxide anion of δ-hydroxy-α,β-unsaturated esters as key steps.

本文言語	英語
ページ（範囲）	109-110
ページ数	2
ジャーナル	Chemistry Letters
号	2
DOI	https://doi.org/10.1246/cl.1998.109
出版ステータス	出版済み - 1998

ASJC Scopus 主題領域

化学一般

文献へのアクセス

10.1246/cl.1998.109

引用スタイル

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title = "Expeditious and stereoselective synthesis of chiral trans -β-hydroxy-δ-lactone systems",

abstract = "Expeditious and stereoselective synthesis of chiral trans-β-hydroxy-δ-lactone systems starting from γ,δ-epoxy acrylates is described which involves the regioselective ring opening of an epoxide and the intramolecular conjugate addition of a hemiacetal alkoxide anion of δ-hydroxy-α,β-unsaturated esters as key steps.",

author = "Masahiro Miyazawa and Erika Matsuoka and Shinobu Sasaki and Satoshi Oonuma and Kimiyuki Maruyama and Masaaki Miyashita",

year = "1998",

doi = "10.1246/cl.1998.109",

language = "英語",

pages = "109--110",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "Oxford University Press",

number = "2",

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TY - JOUR

T1 - Expeditious and stereoselective synthesis of chiral trans -β-hydroxy-δ-lactone systems

AU - Miyazawa, Masahiro

AU - Matsuoka, Erika

AU - Sasaki, Shinobu

AU - Oonuma, Satoshi

AU - Maruyama, Kimiyuki

AU - Miyashita, Masaaki

PY - 1998

Y1 - 1998

N2 - Expeditious and stereoselective synthesis of chiral trans-β-hydroxy-δ-lactone systems starting from γ,δ-epoxy acrylates is described which involves the regioselective ring opening of an epoxide and the intramolecular conjugate addition of a hemiacetal alkoxide anion of δ-hydroxy-α,β-unsaturated esters as key steps.

AB - Expeditious and stereoselective synthesis of chiral trans-β-hydroxy-δ-lactone systems starting from γ,δ-epoxy acrylates is described which involves the regioselective ring opening of an epoxide and the intramolecular conjugate addition of a hemiacetal alkoxide anion of δ-hydroxy-α,β-unsaturated esters as key steps.

UR - http://www.scopus.com/inward/record.url?scp=0001290552&partnerID=8YFLogxK

U2 - 10.1246/cl.1998.109

DO - 10.1246/cl.1998.109

M3 - 学術論文

AN - SCOPUS:0001290552

SN - 0366-7022

SP - 109

EP - 110

JO - Chemistry Letters

JF - Chemistry Letters

IS - 2

ER -

Expeditious and stereoselective synthesis of chiral trans -β-hydroxy-δ-lactone systems

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