Palladium-catalyzed C-allylation of naphthols by direct use of allylic alcohols under neutral conditions

Yuzuki Tada; Akiharu Satake; Isao Shimizu; Akio Yamamoto

Palladium-catalyzed C-allylation of naphthols by direct use of allylic alcohols under neutral conditions

Yuzuki Tada, Akiharu Satake, Isao Shimizu^*, Akio Yamamoto

^*この研究の対応する著者

早稲田大学

研究成果: Article › 査読

26 被引用数 (Scopus)

抄録

C-Allylation of 1-or 2-naphthols to give mono-, di-, and triallylnaphthols selectively using allylic alcohols directly under neutral conditions has been realized by employing palladium catalysis in the presence of molecular sieve 4A. This method is also applicable for the multiple allylation of 2,6-dihydroxynaphthalene.

本文言語	English
ページ（範囲）	1021-1022
ページ数	2
ジャーナル	Chemistry Letters
号	12
出版ステータス	Published - 1996

ASJC Scopus subject areas

化学 (全般)

他のファイルとリンク

引用スタイル

@article{9f3dd2f3be3543698485430535d6ef62,

title = "Palladium-catalyzed C-allylation of naphthols by direct use of allylic alcohols under neutral conditions",

abstract = "C-Allylation of 1-or 2-naphthols to give mono-, di-, and triallylnaphthols selectively using allylic alcohols directly under neutral conditions has been realized by employing palladium catalysis in the presence of molecular sieve 4A. This method is also applicable for the multiple allylation of 2,6-dihydroxynaphthalene.",

author = "Yuzuki Tada and Akiharu Satake and Isao Shimizu and Akio Yamamoto",

year = "1996",

language = "English",

pages = "1021--1022",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "Chemical Society of Japan",

number = "12",

}

TY - JOUR

T1 - Palladium-catalyzed C-allylation of naphthols by direct use of allylic alcohols under neutral conditions

AU - Tada, Yuzuki

AU - Satake, Akiharu

AU - Shimizu, Isao

AU - Yamamoto, Akio

PY - 1996

Y1 - 1996

N2 - C-Allylation of 1-or 2-naphthols to give mono-, di-, and triallylnaphthols selectively using allylic alcohols directly under neutral conditions has been realized by employing palladium catalysis in the presence of molecular sieve 4A. This method is also applicable for the multiple allylation of 2,6-dihydroxynaphthalene.

AB - C-Allylation of 1-or 2-naphthols to give mono-, di-, and triallylnaphthols selectively using allylic alcohols directly under neutral conditions has been realized by employing palladium catalysis in the presence of molecular sieve 4A. This method is also applicable for the multiple allylation of 2,6-dihydroxynaphthalene.

UR - http://www.scopus.com/inward/record.url?scp=0042103128&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0042103128&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0042103128

SN - 0366-7022

SP - 1021

EP - 1022

JO - Chemistry Letters

JF - Chemistry Letters

IS - 12

ER -

Palladium-catalyzed C-allylation of naphthols by direct use of allylic alcohols under neutral conditions

抄録

ASJC Scopus subject areas

他のファイルとリンク

フィンガープリント

引用スタイル