A rapid construction of new boron heterocycles and evaluation of photophysical properties of iminoboronates-Reference-Cited by-同舟云学术

A rapid construction of new boron heterocycles and evaluation of photophysical properties of iminoboronates

Published:2022 Issue:32 Volume:20 Page:6413-6417
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Kuang Qiulin¹,Hu Xueyuan¹,Li Yanwu¹,Shang Suqin¹,Huang Xin¹,Liao Siwei¹,Song Yibo¹,Ma Wanqian¹,Li Suzhen¹,Liu Aqin¹,Liu Xiaoling¹,Zhang Xiuyu¹,Yuan Jianyong¹^ORCID

Affiliation:

1. Department of Medicinal Chemistry, College of Pharmacy, Chongqing Medical University, Chongqing 400016, PR China

Abstract

A green and efficient method for the synthesis of oxadiazaborole, dioxazaborinine, and oxadiazaborinine from the reactions of phenylboronic acid with amidoxime, α-hydroxyl oxime and α-hydroxyl hydrazone, respectively, is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01083F

Reference23 articles.

1. Enhanced Tumor Selectivity of 5-Fluorouracil Using a Reactive Oxygen Species-Activated Prodrug Approach

2. 1,2‐Boryl Migration Enables Efficient Access to Versatile Functionalized Boronates

3. Anticancer boron-containing prodrugs responsive to oxidative stress from the tumor microenvironment

4. ROS-activated anticancer prodrugs: a new strategy for tumor-specific damage

5. Synthesis, characterization, antimicrobial activity, and QSAR studies on substituted oxadiazaboroles

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