2(3H)-and 2(5H)-furanones. VII. Chirality transfer on the tetronic acid templates

Takefumi Momose; Naoki Toyooka; Morihiro Nishio; Hiroyuki Shinoda; Hiromi Fujii; Hironobu Yanagino

doi:10.3987/com-99-8494

2(3H)-and 2(5H)-furanones. VII. Chirality transfer on the tetronic acid templates

Takefumi Momose, Naoki Toyooka^*, Morihiro Nishio, Hiroyuki Shinoda, Hiromi Fujii, Hironobu Yanagino

^*この論文の責任著者

工学科　生命工学コース

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

10 被引用数 (Scopus)

抄録

The chirality transfer on the β-tetronic acid templates has been examined via highly diastereoselective alkylation or the Michael reaction at the α-position of the acids. Synthetic utility of this transfer procedure was demonstrated by the formal synthesis of (+)-cassiol and enantiodivergent synthesis of O-methyljoubertiamine.

本文言語	英語
ページ（範囲）	1321-1343
ページ数	23
ジャーナル	Heterocycles
巻	51
号	6
DOI	https://doi.org/10.3987/com-99-8494
出版ステータス	出版済み - 1999/06/01

ASJC Scopus 主題領域

分析化学
薬理学
有機化学

文献へのアクセス

10.3987/com-99-8494

引用スタイル

@article{f1e4c909f5e74cfba71e48e32bb493b3,

title = "2(3H)-and 2(5H)-furanones. VII. Chirality transfer on the tetronic acid templates",

abstract = "The chirality transfer on the β-tetronic acid templates has been examined via highly diastereoselective alkylation or the Michael reaction at the α-position of the acids. Synthetic utility of this transfer procedure was demonstrated by the formal synthesis of (+)-cassiol and enantiodivergent synthesis of O-methyljoubertiamine.",

author = "Takefumi Momose and Naoki Toyooka and Morihiro Nishio and Hiroyuki Shinoda and Hiromi Fujii and Hironobu Yanagino",

year = "1999",

month = jun,

day = "1",

doi = "10.3987/com-99-8494",

language = "英語",

volume = "51",

pages = "1321--1343",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

number = "6",

}

TY - JOUR

T1 - 2(3H)-and 2(5H)-furanones. VII. Chirality transfer on the tetronic acid templates

AU - Momose, Takefumi

AU - Toyooka, Naoki

AU - Nishio, Morihiro

AU - Shinoda, Hiroyuki

AU - Fujii, Hiromi

AU - Yanagino, Hironobu

PY - 1999/6/1

Y1 - 1999/6/1

N2 - The chirality transfer on the β-tetronic acid templates has been examined via highly diastereoselective alkylation or the Michael reaction at the α-position of the acids. Synthetic utility of this transfer procedure was demonstrated by the formal synthesis of (+)-cassiol and enantiodivergent synthesis of O-methyljoubertiamine.

AB - The chirality transfer on the β-tetronic acid templates has been examined via highly diastereoselective alkylation or the Michael reaction at the α-position of the acids. Synthetic utility of this transfer procedure was demonstrated by the formal synthesis of (+)-cassiol and enantiodivergent synthesis of O-methyljoubertiamine.

UR - http://www.scopus.com/inward/record.url?scp=0033150197&partnerID=8YFLogxK

U2 - 10.3987/com-99-8494

DO - 10.3987/com-99-8494

M3 - 学術論文

AN - SCOPUS:0033150197

SN - 0385-5414

VL - 51

SP - 1321

EP - 1343

JO - Heterocycles

JF - Heterocycles

IS - 6

ER -

2(3H)-and 2(5H)-furanones. VII. Chirality transfer on the tetronic acid templates

抄録

ASJC Scopus 主題領域

文献へのアクセス

フィンガープリント

引用スタイル