Convenient access to readily soluble symmetrical dialkyl-substituted α-oligofurans

Author:

Korshin Edward E.123,Leitus Gregory M.423,Bendikov Michael123

Affiliation:

1. Department of Organic Chemistry

2. Weizmann Institute of Science

3. Rehovot 76100, Israel

4. Department of Chemical Research Support

Abstract

A combination of heteroatom directed lithiation/CuCl2-induced homocoupling, Wittig olefination/Pd-catalyzed transfer hydrogenation followed by Suzuki–Miyaura or Stille cross-coupling enables convenient access to dialkyl-substituted α-oligofurans of potential interest for organic electronics.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

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5. P. Bäuerle , in Electronic Materials: The Oligomer Approach , ed. K. Müllen and G. Wegner , Wiley-VCH , Weinheim , 1998 , pp. 105–197

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