Angewandte Chemie. International edition in English 2014-08-18

The ketene-surrogate coupling: catalytic conversion of aryl iodides into aryl ketenes through ynol ethers.

Wenhan Zhang, Joseph M Ready

Index: Angew. Chem. Int. Ed. Engl. 53(34) , 8980-4, (2014)

Full Text: HTML

Abstract

tert-Butoxyacetylene is shown to undergo Sonogashira coupling with aryl iodides to yield aryl-substituted tert-butyl ynol ethers. These intermediates participate in a [1,5]-hydride shift, which results in the extrusion of isobutylene and the generation of aryl ketenes. The ketenes are trapped in situ with multiple nucleophiles or undergo electrocyclic ring closure to yield hydroxynaphthalenes and quinolines. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.


Related Compounds

Related Articles:

Controlled self-assembly of a pyrene-based bolaamphiphile by acetate ions: from nanodisks to nanofibers by fluorescence enhancement.

2015-06-14

[Soft Matter 11 , 4424-9, (2015)]

Enzymatic primer-extension with glycerol-nucleoside triphosphates on DNA templates.

2009-01-01

[PLoS ONE 4(3) , e4949, (2009)]

Zwitterionic red fluorescent polymeric nanoparticles for cell imaging.

2014-10-01

[Macromol. Biosci. 14(10) , 1361-7, (2014)]

Planar-rotor architecture based pyrene-vinyl-tetraphenylethylene conjugated systems: photophysical properties and aggregation behavior.

2015-11-21

[Org. Biomol. Chem. 13 , 10663-74, (2015)]

Palladium-catalyzed formylation of organic halides with carbon monoxide and tin hydride.

1986-02-01

[J. Am. Chem. Soc. 108 , 452, (1986)]

More Articles...