Directing Group‐Promoted Inert C−O Bond Activation Using Versatile Boronic Acid as a Coupling Agent-Reference-Cited by-同舟云学术

Directing Group‐Promoted Inert C−O Bond Activation Using Versatile Boronic Acid as a Coupling Agent

Published:2020-11-19 Issue:71 Volume:26 Page:17021-17026
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Ambre Ram¹,Wang Ting‐Hsuan¹,Xian Anmei²,Chen Yu‐Shiuan¹,Liang Yu‐Fu¹,Jurca Titel³,Zhao Lili²,Ong Tiow‐Gan¹⁴^ORCID

Affiliation:

1. Institute of Chemistry Academia Sinica Taipei Taiwan) (ROC

2. Institute of Advanced Synthesis School of Chemistry and Molecular Engineering Jiangsu National Synergetic Innovation Center for, Advanced Materials Nanjing Tech University Nanjing 211816 P. R. China

3. Department of Chemistry and the Renewable Energy and Chemical Transformations Cluster University of Central Florida Orlando FL 32816 USA

4. Department of Chemistry National (Taiwan) University Taipei Taiwan) (ROC

Funder

Ministry of Science and Technology

Academia Sinica

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202004132

Reference100 articles.

2. Metal-catalyzed activation of ethers via C–O bond cleavage: a new strategy for molecular diversity

3. An Adventure in Sustainable Cross-Coupling of Phenols and Derivatives via Carbon–Oxygen Bond Cleavage

4. Ruthenium-Catalyzed Conversion of sp3 C–O Bonds in Ethers to C–C Bonds Using Triarylboroxines

5. For example: Oral rat LD50: PhCl (1231 mg kg−1); PhBr (2383 mg kg−1); PhI (1749 mg kg−1); PhOMe (5290 mg kg−1). Source FisherSci/Sigma MSDS.

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