Decarboxylative Suzuki–Miyaura coupling of (hetero)aromatic carboxylic acids using iodine as the terminal oxidant-Reference-Cited by-同舟云学术

Decarboxylative Suzuki–Miyaura coupling of (hetero)aromatic carboxylic acids using iodine as the terminal oxidant

Published:2019 Issue:45 Volume:55 Page:6445-6448
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Quibell Jacob M.¹²³⁴^ORCID,Duan Guojian¹²³⁴⁵,Perry Gregory J. P.¹²³⁴^ORCID,Larrosa Igor¹²³⁴^ORCID

Affiliation:

1. School of Chemistry

2. University of Manchester

3. Manchester

4. UK

5. College of Pharmacy

Abstract

A novel methodology for the decarboxylative Suzuki–Miyaura-type coupling of carboxylic acids with arylboronic acids has been developed.

Funder

National Natural Science Foundation of China

China Scholarship Council

University of Manchester

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CC/C9CC01817D

Reference94 articles.

1. Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction

2. Palladium-Catalyzed Cross-Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize

3. Recent Advances in Palladium-Catalyzed Cross-Coupling Reactions at ppm to ppb Molar Catalyst Loadings

4. The B-Alkyl Suzuki-Miyaura Cross-Coupling Reaction: Development, Mechanistic Study, and Applications in Natural Product Synthesis

5. Palladium-Catalyzed Cross-Coupling Reactions in Total Synthesis

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