Facile Synthesis of -acylhydroxamates Reaction of Oxime Chlorides with Carboxylic Acids
Overview
Overview
Journal
RSC Adv
Publisher
Royal Society of Chemistry
Specialty
Chemistry
Date
2022 May 2
PMID
35494140
Authors
Affiliations
Affiliations
Soon will be listed here.
Abstract
A simple and efficient method for the synthesis of -acylhydroxamate derivatives from oxime chlorides and carboxylic acids was developed. The reaction affords clean and facile access to diverse -acylhydroxamates in high yields (up to 85%). The chemical structure of a typical product was confirmed using single-crystal X-ray structure analysis.
Citing Articles
Wang K, Li Y, Zhang W, Chen R, Ma X, Wang M Molecules. 2022; 27(10).
PMID: 35630538 PMC: 9145198. DOI: 10.3390/molecules27103064.
References
1.
Zhou X, Xu X, Shi Z, Liu K, Gao H, Li W
. Enolate-mediated 1,3-dipolar cycloaddition reaction of β-functionalized ketones with nitrile oxides: direct access to 3,4,5-trisubstituted isoxazoles. Org Biomol Chem. 2016; 14(23):5246-50.
DOI: 10.1039/c6ob00717a.
View
2.
Lam N, Wu K, Yu J
. Advancing the Logic of Chemical Synthesis: C-H Activation as Strategic and Tactical Disconnections for C-C Bond Construction. Angew Chem Int Ed Engl. 2020; 60(29):15767-15790.
PMC: 8177825.
DOI: 10.1002/anie.202011901.
View
3.
Bartlett S, Sohtome Y, Hashizume D, White P, Sawamura M, Johnson J
. Catalytic Enantioselective [3 + 2] Cycloaddition of α-Keto Ester Enolates and Nitrile Oxides. J Am Chem Soc. 2017; 139(25):8661-8666.
PMC: 5547566.
DOI: 10.1021/jacs.7b03782.
View
4.
Li B, Yang J, Xu H, Song H, Wang B
. Rhodium(III)-Catalyzed C-H Activation and Annulation with 1-Alkynylphosphine Sulfides: A Mild and Regioselective Access for the Synthesis of Bulky Phosphine Ligands. J Org Chem. 2015; 80(24):12397-409.
DOI: 10.1021/acs.joc.5b02265.
View
5.
Li W, Zhou X, Shi Z, Liu Y, Liu Z, Gao H
. Enolate-mediated 1,3-dipolar cycloaddition reactions of allyl ketones with nitrile oxides: direct access to 3,5-disubstituted isoxazolines. Org Biomol Chem. 2016; 14(42):9985-9988.
DOI: 10.1039/c6ob02025a.
View