Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction

Hitoshi Abe; Toshitaka Kawai; Yoshinori Komatsu; Mayu Kamimura; Yasuo Takeuchi; Yoshikazu Horino

doi:10.3987/COM-12-S(N)87

Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction

Hitoshi Abe, Toshitaka Kawai, Yoshinori Komatsu, Mayu Kamimura, Yasuo Takeuchi, Yoshikazu Horino

工学科　応用化学コース

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

8 被引用数 (Scopus)

抄録

Neo-tanshinlactone (1) was synthesized by the intramolecular aryl-aryl coupling reaction of the precursor ester, which was prepared from the corresponding furan carboxylic acid (13) and naphthol (3), using a palladium reagent.

本文言語	英語
ページ（範囲）	785-789
ページ数	5
ジャーナル	Heterocycles
巻	86
号	1
DOI	https://doi.org/10.3987/COM-12-S(N)87
出版ステータス	出版済み - 2012

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-12-S(N)87

引用スタイル

@article{92880c182fa546eb966c618de15fe6df,

title = "Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction",

abstract = "Neo-tanshinlactone (1) was synthesized by the intramolecular aryl-aryl coupling reaction of the precursor ester, which was prepared from the corresponding furan carboxylic acid (13) and naphthol (3), using a palladium reagent.",

author = "Hitoshi Abe and Toshitaka Kawai and Yoshinori Komatsu and Mayu Kamimura and Yasuo Takeuchi and Yoshikazu Horino",

year = "2012",

doi = "10.3987/COM-12-S(N)87",

language = "英語",

volume = "86",

pages = "785--789",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

number = "1",

}

TY - JOUR

T1 - Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction

AU - Abe, Hitoshi

AU - Kawai, Toshitaka

AU - Komatsu, Yoshinori

AU - Kamimura, Mayu

AU - Takeuchi, Yasuo

AU - Horino, Yoshikazu

PY - 2012

Y1 - 2012

N2 - Neo-tanshinlactone (1) was synthesized by the intramolecular aryl-aryl coupling reaction of the precursor ester, which was prepared from the corresponding furan carboxylic acid (13) and naphthol (3), using a palladium reagent.

AB - Neo-tanshinlactone (1) was synthesized by the intramolecular aryl-aryl coupling reaction of the precursor ester, which was prepared from the corresponding furan carboxylic acid (13) and naphthol (3), using a palladium reagent.

UR - http://www.scopus.com/inward/record.url?scp=84880645113&partnerID=8YFLogxK

U2 - 10.3987/COM-12-S(N)87

DO - 10.3987/COM-12-S(N)87

M3 - 学術論文

AN - SCOPUS:84880645113

SN - 0385-5414

VL - 86

SP - 785

EP - 789

JO - Heterocycles

JF - Heterocycles

IS - 1

ER -

Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction

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