Visible light mediated azomethine ylide formation - Photoredox catalyzed [3+2] cycloadditions

Magnus Rueping; Daniele Leonori; Thomas Poisson

doi:10.1039/c1cc13660g

Visible light mediated azomethine ylide formation - Photoredox catalyzed [3+2] cycloadditions

Magnus Rueping^*, Daniele Leonori, Thomas Poisson

^*Corresponding author for this work

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

194 Scopus citations

Abstract

The synthesis of highly functionalised N-heterocycles has been achieved by the visible light mediated photoredox conversion of tertiary amines to azomethine ylides and their further reaction with maleimide derivatives as dipolarophiles.

Original language	English (US)
Pages (from-to)	9615-9617
Number of pages	3
Journal	CHEMICAL COMMUNICATIONS
Volume	47
Issue number	34
DOIs	https://doi.org/10.1039/c1cc13660g
State	Published - Sep 14 2011
Externally published	Yes

ASJC Scopus subject areas

Electronic, Optical and Magnetic Materials
General Chemistry
Ceramics and Composites
Metals and Alloys
Materials Chemistry
Surfaces, Coatings and Films
Catalysis

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10.1039/c1cc13660g

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@article{2d7542c7045544d3b779798fd9dcbba1,

title = "Visible light mediated azomethine ylide formation - Photoredox catalyzed [3+2] cycloadditions",

abstract = "The synthesis of highly functionalised N-heterocycles has been achieved by the visible light mediated photoredox conversion of tertiary amines to azomethine ylides and their further reaction with maleimide derivatives as dipolarophiles.",

author = "Magnus Rueping and Daniele Leonori and Thomas Poisson",

year = "2011",

month = sep,

day = "14",

doi = "10.1039/c1cc13660g",

language = "English (US)",

volume = "47",

pages = "9615--9617",

journal = "CHEMICAL COMMUNICATIONS",

issn = "1359-7345",

publisher = "ROYAL SOC CHEMISTRY",

number = "34",

}

TY - JOUR

T1 - Visible light mediated azomethine ylide formation - Photoredox catalyzed [3+2] cycloadditions

AU - Rueping, Magnus

AU - Leonori, Daniele

AU - Poisson, Thomas

PY - 2011/9/14

Y1 - 2011/9/14

N2 - The synthesis of highly functionalised N-heterocycles has been achieved by the visible light mediated photoredox conversion of tertiary amines to azomethine ylides and their further reaction with maleimide derivatives as dipolarophiles.

AB - The synthesis of highly functionalised N-heterocycles has been achieved by the visible light mediated photoredox conversion of tertiary amines to azomethine ylides and their further reaction with maleimide derivatives as dipolarophiles.

UR - http://www.scopus.com/inward/record.url?scp=80051714094&partnerID=8YFLogxK

U2 - 10.1039/c1cc13660g

DO - 10.1039/c1cc13660g

M3 - Article

C2 - 21792444

AN - SCOPUS:80051714094

SN - 1359-7345

VL - 47

SP - 9615

EP - 9617

JO - CHEMICAL COMMUNICATIONS

JF - CHEMICAL COMMUNICATIONS

IS - 34

ER -

Visible light mediated azomethine ylide formation - Photoredox catalyzed [3+2] cycloadditions

Abstract

ASJC Scopus subject areas

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