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  • Sweeney et al. revised Ni C-allylation

    Rights statement: This is the peer reviewed version of the following article: J. B. Sweeney, A. K. Ball, L. J. Smith, Chem. Eur. J. 2018, 24, 7354 which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1002/chem.201801241/abstract This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving.

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Catalytic C-C Bond Formation Using a Simple Nickel Precatalyst System: Base- and Activator-Free Direct C-Allylation by Alcohols and Amines

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Catalytic C-C Bond Formation Using a Simple Nickel Precatalyst System: Base- and Activator-Free Direct C-Allylation by Alcohols and Amines. / Sweeney, Joseph B.; Ball, Anthony K.; Smith, Luke J.
In: Chemistry - A European Journal, Vol. 24, No. 29, 23.05.2018, p. 7354-7357.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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Sweeney JB, Ball AK, Smith LJ. Catalytic C-C Bond Formation Using a Simple Nickel Precatalyst System: Base- and Activator-Free Direct C-Allylation by Alcohols and Amines. Chemistry - A European Journal. 2018 May 23;24(29):7354-7357. Epub 2018 Mar 13. doi: 10.1002/chem.201801241

Author

Sweeney, Joseph B. ; Ball, Anthony K. ; Smith, Luke J. / Catalytic C-C Bond Formation Using a Simple Nickel Precatalyst System : Base- and Activator-Free Direct C-Allylation by Alcohols and Amines. In: Chemistry - A European Journal. 2018 ; Vol. 24, No. 29. pp. 7354-7357.

Bibtex

@article{d31ce23656234cdfa969fa9db87f7446,
title = "Catalytic C-C Bond Formation Using a Simple Nickel Precatalyst System: Base- and Activator-Free Direct C-Allylation by Alcohols and Amines",
abstract = "A {"}totally catalytic{"} nickel(0)-mediated method for base-free direct alkylation of allyl alcohols and allyl amines is reported. The reaction is selective for monoallylation, uses an inexpensive NiII precatalyst system, and requires no activating reagents to be present.",
keywords = "Allylation, C-C bond formation, Nickel, Quaternary, Sustainable chemistry",
author = "Sweeney, {Joseph B.} and Ball, {Anthony K.} and Smith, {Luke J.}",
note = "This is the peer reviewed version of the following article: J. B. Sweeney, A. K. Ball, L. J. Smith, Chem. Eur. J. 2018, 24, 7354 which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1002/chem.201801241/abstract This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving.",
year = "2018",
month = may,
day = "23",
doi = "10.1002/chem.201801241",
language = "English",
volume = "24",
pages = "7354--7357",
journal = "Chemistry - A European Journal",
issn = "0947-6539",
publisher = "Wiley-VCH Verlag",
number = "29",

}

RIS

TY - JOUR

T1 - Catalytic C-C Bond Formation Using a Simple Nickel Precatalyst System

T2 - Base- and Activator-Free Direct C-Allylation by Alcohols and Amines

AU - Sweeney, Joseph B.

AU - Ball, Anthony K.

AU - Smith, Luke J.

N1 - This is the peer reviewed version of the following article: J. B. Sweeney, A. K. Ball, L. J. Smith, Chem. Eur. J. 2018, 24, 7354 which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1002/chem.201801241/abstract This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving.

PY - 2018/5/23

Y1 - 2018/5/23

N2 - A "totally catalytic" nickel(0)-mediated method for base-free direct alkylation of allyl alcohols and allyl amines is reported. The reaction is selective for monoallylation, uses an inexpensive NiII precatalyst system, and requires no activating reagents to be present.

AB - A "totally catalytic" nickel(0)-mediated method for base-free direct alkylation of allyl alcohols and allyl amines is reported. The reaction is selective for monoallylation, uses an inexpensive NiII precatalyst system, and requires no activating reagents to be present.

KW - Allylation

KW - C-C bond formation

KW - Nickel

KW - Quaternary

KW - Sustainable chemistry

U2 - 10.1002/chem.201801241

DO - 10.1002/chem.201801241

M3 - Journal article

AN - SCOPUS:85046016695

VL - 24

SP - 7354

EP - 7357

JO - Chemistry - A European Journal

JF - Chemistry - A European Journal

SN - 0947-6539

IS - 29

ER -