Synthesis of highly oxygenated dinaphthyl ethers via S<inf>N</inf>Ar reactions promoted by Barton's base

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

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Abstract

(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.

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Details

Item Type:	Article
Status:	Published
Creators/Authors:	Creators Email Pitt Username ORCID Wipf, P pwipf@pitt.edu PWIPF Lynch, SM
Date:	3 April 2003
Date Type:	Publication
Journal or Publication Title:	Organic Letters
Volume:	5
Number:	7
Page Range:	1155 - 1158
DOI or Unique Handle:	10.1021/ol034286z
Schools and Programs:	Dietrich School of Arts and Sciences > Chemistry
Refereed:	Yes
ISSN:	1523-7060
MeSH Headings:	Ethers--chemical synthesis; Ethers--chemistry; Guanidine--analogs & derivatives; Guanidine--chemistry; Heterocyclic Compounds with 4 or More Rings--chemical synthesis; Molecular Structure; Naphthalenes--chemistry; Naphthols--chemistry; Oxygen--chemistry; Spiro Compounds
PubMed ID:	12659597
Date Deposited:	31 Jan 2014 21:07
Last Modified:	12 Jun 2021 22:55
URI:	http://d-scholarship-dev.library.pitt.edu/id/eprint/20439

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