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HERO ID
8495701
Reference Type
Journal Article
Title
xxx As di-aryxxx equivalents in polycyclic axxx synthesis
Author(s)
Hart, H; Lai, Cy; Chukuemeka Nwokogu, G; Shamouilian, S
Year
1987
Is Peer Reviewed?
1
Journal
Tetrahedron
ISSN:
0040-4020
Volume
43
Issue
22
Page Numbers
5203-5224
Language
English
DOI
10.1016/S0040-4020(01)87696-1
Abstract
1,2,4,5-Tetrabromobenzenes and analogous napbthalanes react with one or two equivalents of n-butyllithum and various dienes (furans, pyrroles, cyclopentadienes, fulvenes) to form mono- or bis-cycloadducts. Highly substituted arenes can be obtained by removing the oxygen or nitrogens bridges from the furan or pyrrole adducts. By choice of conditions, two identical or two different rings can be fused to the di-aryne epuivalent. Improved short syntheses of permethylnaphthalene, -anthracene and -naphthacene are described. A new triphenylene synthesis is presented. © 1987.
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