Potassium tert-butoxide mediated Heck-type cyclization/isomerization- benzofurans from organocatalytic radical cross-coupling reactions

Magnus Rueping; Matthias Leiendecker; Arindam Das; Thomas Poisson; Lan Bui

doi:10.1039/c1cc14297f

Potassium tert-butoxide mediated Heck-type cyclization/isomerization- benzofurans from organocatalytic radical cross-coupling reactions

Magnus Rueping^*, Matthias Leiendecker, Arindam Das, Thomas Poisson, Lan Bui

^*Corresponding author for this work

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

118 Scopus citations

Abstract

A transition metal-free Heck-type cyclization/isomerization reaction has been developed. Mediated by potassium tert-butoxide and phenanthroline a variety of benzofuran derivatives have been synthesized.

Original language	English (US)
Pages (from-to)	10629-10631
Number of pages	3
Journal	Chemical Communications
Volume	47
Issue number	38
DOIs	https://doi.org/10.1039/c1cc14297f
State	Published - Oct 14 2011
Externally published	Yes

ASJC Scopus subject areas

Metals and Alloys
Materials Chemistry
Surfaces, Coatings and Films
Electronic, Optical and Magnetic Materials
Ceramics and Composites
Catalysis
Chemistry(all)

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@article{9c9f9bc902d242998653d529eee8536e,

title = "Potassium tert-butoxide mediated Heck-type cyclization/isomerization- benzofurans from organocatalytic radical cross-coupling reactions",

abstract = "A transition metal-free Heck-type cyclization/isomerization reaction has been developed. Mediated by potassium tert-butoxide and phenanthroline a variety of benzofuran derivatives have been synthesized.",

author = "Magnus Rueping and Matthias Leiendecker and Arindam Das and Thomas Poisson and Lan Bui",

year = "2011",

month = oct,

day = "14",

doi = "10.1039/c1cc14297f",

language = "English (US)",

volume = "47",

pages = "10629--10631",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "ROYAL SOC CHEMISTRY",

number = "38",

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TY - JOUR

T1 - Potassium tert-butoxide mediated Heck-type cyclization/isomerization- benzofurans from organocatalytic radical cross-coupling reactions

AU - Rueping, Magnus

AU - Leiendecker, Matthias

AU - Das, Arindam

AU - Poisson, Thomas

AU - Bui, Lan

PY - 2011/10/14

Y1 - 2011/10/14

N2 - A transition metal-free Heck-type cyclization/isomerization reaction has been developed. Mediated by potassium tert-butoxide and phenanthroline a variety of benzofuran derivatives have been synthesized.

AB - A transition metal-free Heck-type cyclization/isomerization reaction has been developed. Mediated by potassium tert-butoxide and phenanthroline a variety of benzofuran derivatives have been synthesized.

UR - http://www.scopus.com/inward/record.url?scp=80052948467&partnerID=8YFLogxK

U2 - 10.1039/c1cc14297f

DO - 10.1039/c1cc14297f

M3 - Article

C2 - 21892507

AN - SCOPUS:80052948467

SN - 1359-7345

VL - 47

SP - 10629

EP - 10631

JO - Chemical Communications

JF - Chemical Communications

IS - 38

ER -

Potassium tert-butoxide mediated Heck-type cyclization/isomerization- benzofurans from organocatalytic radical cross-coupling reactions

Abstract

ASJC Scopus subject areas

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