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

Yuzuki Tada, Akiharu Satake, Isao Shimizu, Akio Yamamoto

Research output: Contribution to journalArticle

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 languageEnglish
Pages (from-to)1021-1022
Number of pages2
JournalChemistry Letters
Issue number12
Publication statusPublished - 1996

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Allylation
Naphthols
Palladium
Molecular sieves
Catalysis
allyl alcohol

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Palladium-catalyzed C-allylation of naphthols by direct use of allylic alcohols under neutral conditions. / Tada, Yuzuki; Satake, Akiharu; Shimizu, Isao; Yamamoto, Akio.

In: Chemistry Letters, No. 12, 1996, p. 1021-1022.

Research output: Contribution to journalArticle

Tada, Yuzuki ; Satake, Akiharu ; Shimizu, Isao ; Yamamoto, Akio. / Palladium-catalyzed C-allylation of naphthols by direct use of allylic alcohols under neutral conditions. In: Chemistry Letters. 1996 ; No. 12. pp. 1021-1022.
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