Functionalized Naphthalenes by Benzotriazole-Mediated Annulation

Alan R. Katritzky; Guifen Zhang; Linghong Xie

doi:10.1080/00397919708005917

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Functionalized Naphthalenes by Benzotriazole-Mediated Annulation

Journal article

Peer reviewed

Functionalized Naphthalenes by Benzotriazole-Mediated Annulation

Alan R. Katritzky, Guifen Zhang and Linghong Xie

Synthetic communications, Vol.27(22), pp.3951-3961

01/11/1997

DOI: https://doi.org/10.1080/00397919708005917

Abstract

The anions of 3-benzotriazolylphthalide (1) and of 2-(benzotriazolylmethyl)benzonitrile (6) condense regioselectively with a range of Michael acceptors to form 1,4-dihydroxynaphthalenes 4b-f and 1-amino-2,3-di(methoxycarbonyl)naphthalene (9) in moderate to good yields.

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Title: Functionalized Naphthalenes by Benzotriazole-Mediated Annulation
Creators - without role: Alan R. Katritzky - Center for Heterocyclic Compounds, Department of Chemistry , University of Florida
Guifen Zhang - Center for Heterocyclic Compounds, Department of Chemistry , University of Florida
Linghong Xie - Center for Heterocyclic Compounds, Department of Chemistry , University of Florida
Publication Details: Synthetic communications, Vol.27(22), pp.3951-3961
Publisher: Taylor & Francis Group
Identifiers: 9938542408331
Academic Unit: King Abdulaziz University
Language: English
Resource Type: Journal article