A novel approach to a one-pot synthesis of unsubstituted oligo(α-thiophenes)

Ludmila Buzhansky; Ben Ami Feit

doi:10.1021/jo025838e

A novel approach to a one-pot synthesis of unsubstituted oligo(α-thiophenes)

Ludmila Buzhansky, Ben Ami Feit^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

6 Scopus citations

Abstract

Oligo(α-thiophenes) α-4T and α-8T were prepared by the following one-pot sequential conversions: thiophene (T) → α-2T → α-4T → α-8T. PdCl₂-induced coupling of a mono-α-mercuration derivative of each of the n-mers T, α-2T, and α-4T was applied in these conversions.

Original language	English
Pages (from-to)	7523-7525
Number of pages	3
Journal	Journal of Organic Chemistry
Volume	67
Issue number	21
DOIs	https://doi.org/10.1021/jo025838e
State	Published - 18 Oct 2002

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abstract = "Oligo(α-thiophenes) α-4T and α-8T were prepared by the following one-pot sequential conversions: thiophene (T) → α-2T → α-4T → α-8T. PdCl2-induced coupling of a mono-α-mercuration derivative of each of the n-mers T, α-2T, and α-4T was applied in these conversions.",

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N2 - Oligo(α-thiophenes) α-4T and α-8T were prepared by the following one-pot sequential conversions: thiophene (T) → α-2T → α-4T → α-8T. PdCl2-induced coupling of a mono-α-mercuration derivative of each of the n-mers T, α-2T, and α-4T was applied in these conversions.

AB - Oligo(α-thiophenes) α-4T and α-8T were prepared by the following one-pot sequential conversions: thiophene (T) → α-2T → α-4T → α-8T. PdCl2-induced coupling of a mono-α-mercuration derivative of each of the n-mers T, α-2T, and α-4T was applied in these conversions.

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A novel approach to a one-pot synthesis of unsubstituted oligo(α-thiophenes)

Abstract

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