Tetrahedron letters

A new approach to dihydrobenzofurans by intramolecular trapping of benzynes by hydroxyl functions

MA Birkett, DW Knight, MB Mitchell

Index: Birkett, Michael A.; Knight, David W.; Mitchell, Michael B. Tetrahedron Letters, 1993 , vol. 34, # 43 p. 6939 - 6940

Full Text: HTML

Citation Number: 17

Abstract

Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... The adducts 3, derived from condensations of the 1-aminobenzotriazole dianion 2 and aldehydes or ketones, are converted into the corresponding benzynes upon exposure to either -bromosuccinimide or lead(IV) acetate; intramolecular trapping by the hydroxyl group then leads to the ...

Related Articles:

An Improved Palladium-Catalyzed Conversion of Aryl and Vinyl Triflates to Bromides and Chlorides

[Pan, Jun; Wang, Xinyan; Zhang, Yong; Buchwald, Stephen L. Organic Letters, 2011 , vol. 13, # 18 p. 4974 - 4976]

… and dihydrobenzopyrans (chromans) based on the intramolecular trapping by alcohols of benzynes generated from 7-substituted-1-aminobenzotriazoles

[Birkett, Michael A.; Knight, David W.; Little, Paul B.; Mitchell, Michael B. Tetrahedron, 2000 , vol. 56, # 7 p. 1013 - 1023]

More Articles...