CoCl(PPh3)3 as Cyclotrimerization Catalyst for Functionalized Triynes under Mild Conditions

Phillip Jungk; Fabian Fischer; Indre Thiel; Marko Hapke

doi:10.1021/acs.joc.5b01623

CoCl(PPh3)3 as Cyclotrimerization Catalyst for Functionalized Triynes under Mild Conditions

Phillip Jungk, Fabian Fischer, Indre Thiel, Marko Hapke

Institute of Catalysis

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

Abstract

The ubiquitary Co(I) complex CoCl(PPh3)3 was found to be a convenient catalyst for the [2 + 2 + 2] cycloaddition of functionalized triynes under mild reaction conditions and devoid of any additional additive, yielding the substituted arene compounds. Successful development of synthetic routes to various triynes and the subsequent cyclotrimerization key step gave systematic access to a variety of different bi- and triaryls with good to excellent yields for the cyclization.

Original language	English
Pages (from-to)	9781-9793
Number of pages	13
Journal	The Journal of Organic Chemistry
Volume	80
DOIs	https://doi.org/10.1021/acs.joc.5b01623
Publication status	Published - 2015

Fields of science

104 Chemistry

Access to Document

10.1021/acs.joc.5b01623

Cite this

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title = "CoCl(PPh3)3 as Cyclotrimerization Catalyst for Functionalized Triynes under Mild Conditions",

abstract = "The ubiquitary Co(I) complex CoCl(PPh3)3 was found to be a convenient catalyst for the [2 + 2 + 2] cycloaddition of functionalized triynes under mild reaction conditions and devoid of any additional additive, yielding the substituted arene compounds. Successful development of synthetic routes to various triynes and the subsequent cyclotrimerization key step gave systematic access to a variety of different bi- and triaryls with good to excellent yields for the cyclization.",

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journal = "The Journal of Organic Chemistry",

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AU - Fischer, Fabian

AU - Thiel, Indre

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AB - The ubiquitary Co(I) complex CoCl(PPh3)3 was found to be a convenient catalyst for the [2 + 2 + 2] cycloaddition of functionalized triynes under mild reaction conditions and devoid of any additional additive, yielding the substituted arene compounds. Successful development of synthetic routes to various triynes and the subsequent cyclotrimerization key step gave systematic access to a variety of different bi- and triaryls with good to excellent yields for the cyclization.

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DO - 10.1021/acs.joc.5b01623

M3 - Article

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JO - The Journal of Organic Chemistry

JF - The Journal of Organic Chemistry

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