Synthesis of New Lipophilic Rosin-based Methanofullerenes from Bromoand Chloromethylketones N-substituted Proteinogenic Amino Acids

Author(s): Ilshat M. Sakhautdinov*, Rauilya N. Malikova, Oksana V. Akchurina, Svetlana F. Petrova, Marat S. Yunusov

Journal Name: Letters in Organic Chemistry

Volume 14 , Issue 8 , 2017

Become EABM
Become Reviewer
Call for Editor

Graphical Abstract:


Background: Synthesis of lipophilic mitochondria-targeted antioxidants is a topical problem of modern biochemistry. The so-called "radical sponges" effect is a very high ability of fullerene C60 and its derivatives to catch free radicals. The experiments showed that the fullerene derivatives increase resistance of animals towards oxidative stress and prevent passing of neurodegenerative processes.

Objective: Synthesis of lipophilic fullerene C60 conjugates based on maleopimaric acid derived from resin.

Methods: Synthesis of new diterpene containing fullerene C60 conjugates based on the bromo- and chloromethylketones by primary functionalization of the fullerene core by the Bingel cyclopropanation reaction was shown. Bromo- and chloromethylketones were obtained from methyl maleopimarateproteinogenic amino acids condensation products by the Arndt-Eistert reaction.

Results: Diazoketones and chloromethylketones were received from carboxylic acids and corresponding chlorides under Arndt-Eistert reaction conditions. Chloromethylketones formed due to a Nierenstein side reaction. The IR spectra of diazo compounds 2a-e contained a strong absorption band for the diazo group at 2103-2115 cm–1. The reaction of diazoketones with HBr produced bromomethylketones in excellent yield. Bromo- and chloromethylketones were reacted with fullerene C60 in the presence of 1,8-diazabicyclo(5.4.0)undec-7-ene (DBU) in toluene to give diterpene containing fullerene conjugates. Fullerene conjugates formed 6% oil solutions in different sunflower oils. The structures of all compounds obtained were proved using 2D NMR HSQC, HMBC, COSY, NOESY experiments.

Conclusion: Rosin-based methanofullerenes were synthesized for the first time under Bingel conditions by [2+1]-cyclopropanation of the chloro- and bromomethylketones to fullerene C60 in the presence of DBU. In our case chloromethylketones gave better yields in the Bingel reaction than bromomethylketones. The obtained diterpene containing fullerene conjugates have the ability to dissolve in sunflower oils.

Keywords: [2+1]-cycloaddition, the Arndt-Eistert reaction, methyl maleopimarate, methanofullerenes, the Bingel reaction, amino acids.

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2017
Published on: 13 June, 2017
Page: [575 - 584]
Pages: 10
DOI: 10.2174/1570178614666170614091621
Price: $65

Article Metrics

PDF: 14