Synthesis of Arylpalladium(II) Boronates: Confirming the Structure and Chemical Competence of Pre‐transmetalation Intermediates in the Suzuki–Miyaura Reaction-Reference-Cited by-同舟云学术

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Synthesis of Arylpalladium(II) Boronates: Confirming the Structure and Chemical Competence of Pre‐transmetalation Intermediates in the Suzuki–Miyaura Reaction

Published:2021-05-26 Issue:27 Volume:133 Page:15023-15027
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Olding Angus¹,Ho Curtis C.¹^ORCID,Canty Allan J.¹^ORCID,Lucas Nigel T.²^ORCID,Horne James³,Bissember Alex C.¹^ORCID

Affiliation:

1. School of Natural Sciences—Chemistry University of Tasmania Hobart Tasmania Australia

2. Department of Chemistry University of Otago Dunedin, Otago New Zealand

3. Central Science Laboratory University of Tasmania Hobart Tasmania Australia

Funder

Australian Research Council

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202104802

Reference27 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. Selection of boron reagents for Suzuki–Miyaura coupling

4. Enantiospecific and Iterative Suzuki–Miyaura Cross-Couplings

5. Carbon–carbon bonding made easy

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