Related Experiment Video
Updated: Aug 19, 2026
![Solid-phase Synthesis of [4.4] Spirocyclic Oximes](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F58508.jpg&w=3840&q=50)
Solid-phase Synthesis of [4.4] Spirocyclic Oximes
Published on: February 6, 2019
Structural characterization of two novel oxidative derivatives of cyclosporine generated by a chemical method
1Department of Clinical Biochemistry, University of Toronto, Ontario, Canada.
Objectives:
To study the generation of cyclosporine derivatives (CMs) by chemical oxidation of the parent compound using hydrogen peroxide.
Methods And Results:
Hydrogen peroxide was added to cyclosporine (CsA), which was dissolved in ether. After liquid-liquid extraction, CMs were purified by high performance liquid chromatography (HPLC). Detailed structures of CMs were determined by fast atomic bombardment mass spectrometry (FABMS) and nuclear magnetic resonance spectroscopy (NMR). Our results indicated that the parent compound was modified at amino acid number 1 by hydroxylation of the carbon and the formation of a tetrahydrofuran five member ring structure. In addition, these two oxidative products of CsA were determined to be isomeric to each other, differing only in the configuration at one or more carbon atoms. This modification is in contrast to that observed for the formation of the cyclic metabolite of CsA, namely AM1c, by cytochrome P-450 isoenzymes, where the addition of the hydroxyl group occurs on the carbon of amino acid 1.
Conclusion:
3 to 4 mg of 2 oxidative derivatives could be produced from 5 mg of CsA by chemical modification of the parent compound. In comparison, biotransformation using the drug-induced hepatic microsomal enzyme system could only produce 0.5 to 1 mg of metabolites/derivatives from 5 mg of CsA.
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Oxidations of Aldehydes and Ketones to Carboxylic Acids
Aldehydes readily undergo oxidation in strong oxidizing agents such as potassium permanganate and chromic acid. The oxidation can also be carried out using mild oxidizing agents such as silver oxide. In fact, aldehydes can be easily oxidized...
Cycloaddition Reactions: Overview
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
Cycloaddition Reactions: MO Requirements for Thermal Activation
![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
