Borylation of phenols using sulfuryl fluoride activation-Reference-Cited by-同舟云学术

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Borylation of phenols using sulfuryl fluoride activation

Published:2023 Issue:20 Volume:25 Page:7998-8006
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Chen Zhengjun¹,Liu Yan¹,Zeng Chunhua¹,Ren Changyue¹,Li Hongyu¹^ORCID,Jagadeesh Rajenahally V.²³^ORCID,Yuan Zeli¹,Li Xinmin¹²^ORCID

Affiliation:

1. College of Pharmacy, Zunyi Medical University, Zunyi, Guizhou 563003, China

2. Leibniz-Leibniz-Institut für Katalyse e.V., Albert-Einstein-Straße 29A, 18059 Rostock, Germany

3. Nanotechnology Centre, Centre for Energy and Environmental Technologies, VŠB–Technical University of Ostrava, Ostrava-Poruba, Czech Republic

Abstract

Pd-catalyzed borylation of phenols via SO2F2 activation is presented for the synthesis of aryl/heteroaryl boronic esters, selected drug molecules and natural product derivatives as well as a novel boronate-based fluorescent probe HTCPB.

Funder

National Natural Science Foundation of China

Guizhou Science and Technology Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/GC/D3GC01923C

Reference71 articles.

1. Organoborates in new synthetic reactions

2. Methodologies and Strategies for Selective Borylation of C–Het and C–C Bonds

3. A new avenue for the preparation of organoboron compounds via nickel catalysis

4. Selection of boron reagents for Suzuki–Miyaura coupling

5. Aryl Boronic Esters Are Stable on Silica Gel and Reactive under Suzuki–Miyaura Coupling Conditions

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