A rapid access to biaryl ether containing macrocycles by pairwise use of Ugi 4CR and intramolecular SNAr-based cycloetherification

Citation
P. Cristau et al., A rapid access to biaryl ether containing macrocycles by pairwise use of Ugi 4CR and intramolecular SNAr-based cycloetherification, ORG LETT, 3(25), 2001, pp. 4079-4082
Citations number
49
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
3
Issue
25
Year of publication
2001
Pages
4079 - 4082
Database
ISI
SICI code
1523-7060(200112)3:25<4079:ARATBE>2.0.ZU;2-G
Abstract
[GRAPHICS] From readily accessible starting materials, macrocycles with an endo aryl-a ryl ether bond are synthesized in only two operations by combination of the Ugi four-component reaction and an intramolecular: SNAr reaction. The nitr o group serves as an activator for the macrocyclization and provides a hand le for the introduction of functional group diversity. A Ugi reaction promo ted by ammonium chloride In aprotic solvent is documented for the first tim e.