Convenient, tandem and one-reaction vessel synthesis of mixed dialkylated 2-naphthols from 2-tetralone-Reference-Cited by-同舟云学术

Convenient, tandem and one-reaction vessel synthesis of mixed dialkylated 2-naphthols from 2-tetralone

Published:2003-04-01 Issue:4 Volume:81 Page:293-296
ISSN:0008-4042
Container-title:Canadian Journal of Chemistry
language:en
Short-container-title:Can. J. Chem.

Author:

Jha Amitabh,Dimmock Jonathan R

Abstract

A convenient acid-catalyzed method for the synthesis of 1-alkyl-2-alkoxynaphthalenes by one-reaction vessel mixed alkylation of 2-tetralone, using aryl or alkyl aldehydes and alcohols followed by aromatization, is described.Key words: ethers, aromatization, rearrangement, alkylation, 2-alkoxynaphthalenes.

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

Link

http://www.nrcresearchpress.com/doi/pdf/10.1139/v03-064

Reference16 articles.

1. Palladium-catalyzed coupling reaction of 4-alkylnitrobenzenes with aryl bromides at their benzylic position

2. N ‐[α‐( o ‐ and p ‐Methoxyaryl)alkyl]benzotriazoles: Preparation and Use in Synthesis

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