Annelation of perfluorinated heteroaromatic systems by 1,3-dicarbonyl derivatives

Matthew W. Cartwright; Emma L. Parks; Graham Pattison; Rachel Slater; Graham Sandford; Ian Wilson; Dmitrii S. Yufit; Judith A.K. Howard; John A. Christopher; David D. Miller

doi:10.1016/j.tet.2010.02.083

Annelation of perfluorinated heteroaromatic systems by 1,3-dicarbonyl derivatives

Matthew W. Cartwright, Emma L. Parks, Graham Pattison, Rachel Slater, Graham Sandford, Ian Wilson, Dmitrii S. Yufit, Judith A.K. Howard, John A. Christopher, David D. Miller

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

Abstract

Reactions of various perfluorinated heteroaromatic substrates such as tetrafluoro-4-cyanopyridine, tetrafluoropyrazine and tetrafluoropyridazine with 1,3-dicarbonyl systems gave corresponding [5,6]-ring fused furo derivatives. Subsequent reactions of the [5,6] bicyclic scaffolds with nucleophiles gave some highly functionalised heteroaromatic systems.

Original language	English
Pages (from-to)	3222-3227
Number of pages	6
Journal	Tetrahedron
Volume	66
Issue number	17
DOIs	https://doi.org/10.1016/j.tet.2010.02.083
Publication status	Published - 24 Apr 2010

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10.1016/j.tet.2010.02.083

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title = "Annelation of perfluorinated heteroaromatic systems by 1,3-dicarbonyl derivatives",

abstract = "Reactions of various perfluorinated heteroaromatic substrates such as tetrafluoro-4-cyanopyridine, tetrafluoropyrazine and tetrafluoropyridazine with 1,3-dicarbonyl systems gave corresponding [5,6]-ring fused furo derivatives. Subsequent reactions of the [5,6] bicyclic scaffolds with nucleophiles gave some highly functionalised heteroaromatic systems.",

author = "Cartwright, {Matthew W.} and Parks, {Emma L.} and Graham Pattison and Rachel Slater and Graham Sandford and Ian Wilson and Yufit, {Dmitrii S.} and Howard, {Judith A.K.} and Christopher, {John A.} and Miller, {David D.}",

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AU - Cartwright, Matthew W.

AU - Parks, Emma L.

AU - Pattison, Graham

AU - Slater, Rachel

AU - Sandford, Graham

AU - Wilson, Ian

AU - Yufit, Dmitrii S.

AU - Howard, Judith A.K.

AU - Christopher, John A.

AU - Miller, David D.

PY - 2010/4/24

Y1 - 2010/4/24

N2 - Reactions of various perfluorinated heteroaromatic substrates such as tetrafluoro-4-cyanopyridine, tetrafluoropyrazine and tetrafluoropyridazine with 1,3-dicarbonyl systems gave corresponding [5,6]-ring fused furo derivatives. Subsequent reactions of the [5,6] bicyclic scaffolds with nucleophiles gave some highly functionalised heteroaromatic systems.

AB - Reactions of various perfluorinated heteroaromatic substrates such as tetrafluoro-4-cyanopyridine, tetrafluoropyrazine and tetrafluoropyridazine with 1,3-dicarbonyl systems gave corresponding [5,6]-ring fused furo derivatives. Subsequent reactions of the [5,6] bicyclic scaffolds with nucleophiles gave some highly functionalised heteroaromatic systems.

UR - http://www.scopus.com/inward/record.url?scp=77950041857&partnerID=8YFLogxK

U2 - 10.1016/j.tet.2010.02.083

DO - 10.1016/j.tet.2010.02.083

M3 - Article

AN - SCOPUS:77950041857

SN - 0040-4020

VL - 66

SP - 3222

EP - 3227

JO - Tetrahedron

JF - Tetrahedron

IS - 17

ER -

Annelation of perfluorinated heteroaromatic systems by 1,3-dicarbonyl derivatives

Abstract

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