Aldehydes and ketones influence reactivity and selectivity in nickel-catalysed Suzuki–Miyaura reactions-Reference-Cited by-同舟云学术

Aldehydes and ketones influence reactivity and selectivity in nickel-catalysed Suzuki–Miyaura reactions

Published:2020 Issue:7 Volume:11 Page:1905-1911
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Cooper Alasdair K.¹²³⁴,Leonard David K.¹²³⁴^ORCID,Bajo Sonia¹²³⁴,Burton Paul M.⁵⁶⁷⁴,Nelson David J.¹²³⁴^ORCID

Affiliation:

1. WestCHEM Department of Pure and Applied Chemistry

2. University of Strathclyde

3. Glasgow

4. UK

5. Syngenta

6. Jealott's Hill International Research Centre

7. Bracknell

Abstract

Aldehydes and ketones can have beneficial or detrimental effects on nickel-catalysed reactions. When present on the aryl halide, excellent site-selectivity can be achieved; when present as additives, they inhibit the reaction.

Funder

Engineering and Physical Sciences Research Council

Carnegie Trust for the Universities of Scotland

University of Strathclyde

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/SC/C9SC05444H

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