relation: http://d-scholarship-dev.library.pitt.edu/20439/
title: Synthesis of highly oxygenated dinaphthyl ethers via S<inf>N</inf>Ar reactions promoted by Barton's base
creator: Wipf, P
creator: Lynch, SM
description: (Matrix presented) Electron-rich dinaphthyl ethers were synthesized by SNAr reactions between naphthols and activated fluoronaphthalenes. 2-tert-Butyl-1,1,3,3-tetramethylguanidine (Barton's base) was found to be an excellent, mild alternative to traditional inorganic bases for promoting the coupling reaction.
date: 2003-04-03
type: Article
type: PeerReviewed
format: text/plain
language: en
rights: attached
identifier: http://d-scholarship-dev.library.pitt.edu/20439/1/licence.txt
identifier:   Wipf, P and Lynch, SM  (2003) Synthesis of highly oxygenated dinaphthyl ethers via S<inf>N</inf>Ar reactions promoted by Barton's base.  Organic Letters, 5 (7).  1155 - 1158.  ISSN 1523-7060     
relation: 10.1021/ol034286z