One-pot ipso-hydroxylation and ortho-/para-halogenation of (hetero)arylboronic acids under tungsten catalysis-Reference-Cited by-同舟云学术

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One-pot ipso-hydroxylation and ortho-/para-halogenation of (hetero)arylboronic acids under tungsten catalysis

Published:2024 Issue:3 Volume:11 Page:717-725
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Chen Zhilong¹²^ORCID,Kang Jiao¹

Affiliation:

1. School of pharmacy, Tongji medical school, Huazhong university of science and technology, 13# Hangkong Road, Wuhan, 430030, China

2. Key Laboratory of Tropical Medicinal Plant Chemistry of Hainan Province, Hainan Normal University, China

Abstract

The one-pot ipso-hydroxylation-(decarboxylative)-halogenation of (hetero)aryl boronic acids under mild conditions has been developed, in which the (hetero)aryl boronic acids also promoted the reaction by releasing B(OH)3 as a Lewis acid for H2O2, hypohalite and tungsten catalyst.

Funder

Huazhong University of Science and Technology

Hainan Normal University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO01455J

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4. Phenols in Pharmaceuticals: Analysis of a Recurring Motif

5. S. O.Duke and F. E.Dayan , 4.03 - Bioactivity of herbicides , in comprehensive biotechnology , ed. M. Moo-Young , Academic Press , 2nd edn, 2011

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