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

^*Corresponding author for this work

Waseda University

Research output: Contribution to journal › Article › peer-review

26 Citations (Scopus)

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.

Original language	English
Pages (from-to)	1021-1022
Number of pages	2
Journal	Chemistry Letters
Issue number	12
Publication status	Published - 1996

ASJC Scopus subject areas

Chemistry(all)

Cite this

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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",

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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.

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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

Abstract

ASJC Scopus subject areas

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