Highly nucleophilic dipropanolamine chelated boron reagents for aryl-transmetallation to iron complexes-Reference-Cited by-同舟云学术

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Highly nucleophilic dipropanolamine chelated boron reagents for aryl-transmetallation to iron complexes

Published:2015 Issue:47 Volume:44 Page:20577-20583
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Dunsford Jay J.¹²³,Clark Ewan R.¹²³,Ingleson Michael J.¹²³

Affiliation:

1. School of Chemistry

2. University of Manchester

3. UK

Abstract

New arylborates chelated by dipropanolamine are readily synthesised from boronic acids and demonstrated to be highly nucleophilic reagents.

Funder

Leverhulme Trust

European Research Council

Engineering and Physical Sciences Research Council

Royal Society

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/DT/C5DT03835A

Reference54 articles.

1. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst

2. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides

3. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

4. Transmetalation in the Suzuki-Miyaura Coupling: The Fork in the Trail

5. E. Negishi , Hand-book of Organopalladium Chemistry for Organic Synthesis, Wiley, New York, 2002

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3. Protection of Boronic Acids Using a Tridentate Aminophenol ONO Ligand for Selective Suzuki–Miyaura Coupling;The Journal of Organic Chemistry;2023-01-25

4. Iron Catalysis: A New Horizon Towards Organoboron‐mediated C−C Cross‐coupling;Chemistry – An Asian Journal;2022-11-02

5. Cobalt-Catalyzed Coupling of Aryl Chlorides with Aryl Boron Esters Activated by Alkoxides;ACS Catalysis;2021-03-12

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