Direct arylation of C60Cl6 and C70Cl8 with carboxylic acids: a synthetic avenue to water-soluble fullerene derivatives with promising antiviral activity-Reference-Cited by-同舟云学术

Direct arylation of C60Cl6 and C70Cl8 with carboxylic acids: a synthetic avenue to water-soluble fullerene derivatives with promising antiviral activity

Published:2020 Issue:8 Volume:56 Page:1179-1182
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Kraevaya Olga A.¹²³⁴⁵^ORCID,Peregudov Alexander S.⁶²³,Godovikov Ivan A.⁶²³,Shchurik Elena V.⁴⁵³,Martynenko Vyacheslav M.⁴⁵³,Shestakov Alexander F.⁴⁵³⁷⁸,Balzarini Jan⁷⁸⁹³¹⁰,Schols Dominique¹⁰¹¹¹²¹³^ORCID,Troshin Pavel A.¹²³⁴⁵^ORCID

Affiliation:

1. Skolkovo Institute of Science and Technology

2. Moscow

3. Russia

4. IPCP RAS

5. Chernogolovka

6. INEOS RAS

7. Faculty of Fundamental Physics & Chemical Engineering

8. Moscow Lomonosov State University

9. Moscow 119991

10. Rega Institute for Medical Research

11. KU Leuven

12. 3000 Leuven

13. Belgium

Abstract

Unprecedented Friedel–Crafts arylation of chlorofullerenes C₆₀Cl₆ and C₇₀Cl₈ with unprotected carboxylic acids has been utilized for efficient single-step synthesis of the inherently stable water-soluble fullerene derivatives.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/CC/C9CC08400B

Reference33 articles.

1. Gene delivery with polycationic fullerene hexakis-adducts

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