| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273993 | Tetrahedron Letters | 2013 | 5 Pages |
Abstract
A new route for the synthesis of alkyloxy stilbenes from hydroxy benzaldehydes is developed by a combination of one-pot reactions. Tandem one-pot O-alkylation-Wittig and O-alkylation-Wittig-Heck reactions offer a simple access to conjugated alkyloxy stilbenes. A highly conjugated tetra(p-alkyloxystyryl)benzene was synthesized from 1,2,4,5-tetrabromobenzene involving a series of one-pot operations following the O-alkylation-Wittig-Heck scheme.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Krupa N. Patel, Bola V. Kamath, Ashutosh V. Bedekar,