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A valuable upgrade to the portfolio of cycloaddition reactions

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A valuable upgrade to the portfolio of cycloaddition reactions. / Walton, John C.

In: Angewandte Chemie International Edition, Vol. 55, No. 25, 09.06.2016, p. 7034-7036.

Research output: Research - peer-reviewArticle

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Walton, JC 2016, 'A valuable upgrade to the portfolio of cycloaddition reactions' Angewandte Chemie International Edition, vol 55, no. 25, pp. 7034-7036. DOI: 10.1002/anie.201602891

APA

Walton, J. C. (2016). A valuable upgrade to the portfolio of cycloaddition reactions. Angewandte Chemie International Edition, 55(25), 7034-7036. DOI: 10.1002/anie.201602891

Vancouver

Walton JC. A valuable upgrade to the portfolio of cycloaddition reactions. Angewandte Chemie International Edition. 2016 Jun 9;55(25):7034-7036. Available from, DOI: 10.1002/anie.201602891

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Walton, John C./ A valuable upgrade to the portfolio of cycloaddition reactions. In: Angewandte Chemie International Edition. 2016 ; Vol. 55, No. 25. pp. 7034-7036

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@article{e1720ea7227148f6bab43b97abda15b7,
title = "A valuable upgrade to the portfolio of cycloaddition reactions",
abstract = "Recently Antonchick and Manna described a unique annulation that knits together three acetophenones to construct cyclopropanes. The cascade is mediated by organo-copper and free radical species and amounts to the first known [1+1+1] cyclotrimerization. It works well for ketones having electron-deficient or electron-rich substituents in their aryl rings.",
keywords = "Carbocycles, Copper, Cyclotrimerization, Radicals, Synthetic methods",
author = "Walton, {John C.}",
note = "The author thanks EaStCHEM for financial support.",
year = "2016",
month = "6",
doi = "10.1002/anie.201602891",
volume = "55",
pages = "7034--7036",
journal = "Angewandte Chemie International Edition",
issn = "1433-7851",
publisher = "Wiley-Blackwell",
number = "25",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - A valuable upgrade to the portfolio of cycloaddition reactions

AU - Walton,John C.

N1 - The author thanks EaStCHEM for financial support.

PY - 2016/6/9

Y1 - 2016/6/9

N2 - Recently Antonchick and Manna described a unique annulation that knits together three acetophenones to construct cyclopropanes. The cascade is mediated by organo-copper and free radical species and amounts to the first known [1+1+1] cyclotrimerization. It works well for ketones having electron-deficient or electron-rich substituents in their aryl rings.

AB - Recently Antonchick and Manna described a unique annulation that knits together three acetophenones to construct cyclopropanes. The cascade is mediated by organo-copper and free radical species and amounts to the first known [1+1+1] cyclotrimerization. It works well for ketones having electron-deficient or electron-rich substituents in their aryl rings.

KW - Carbocycles

KW - Copper

KW - Cyclotrimerization

KW - Radicals

KW - Synthetic methods

U2 - 10.1002/anie.201602891

DO - 10.1002/anie.201602891

M3 - Article

VL - 55

SP - 7034

EP - 7036

JO - Angewandte Chemie International Edition

T2 - Angewandte Chemie International Edition

JF - Angewandte Chemie International Edition

SN - 1433-7851

IS - 25

ER -

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ID: 243626246