Volume 129, Issue 10 pp. 2748-2752
Zuschrift

Individual (f,tA)- and (f,tC)-Fullerene-Based Nickel(II) Glycinates: Protected Chiral Amino Acids Directly Linked to a Chiral π-Electron System

Dr. Oleg A. Levitskiy

Dr. Oleg A. Levitskiy

Chemistry Department, Lomonosov Moscow State University, Leninskie Gory 1/3, Moscow, Russia

Search for more papers by this author
Dr. Yuri K. Grishin

Dr. Yuri K. Grishin

Chemistry Department, Lomonosov Moscow State University, Leninskie Gory 1/3, Moscow, Russia

Search for more papers by this author
Dr. Olesya O. Semivrazhskaya

Dr. Olesya O. Semivrazhskaya

Chemistry Department, Lomonosov Moscow State University, Leninskie Gory 1/3, Moscow, Russia

Search for more papers by this author
Dr. Asmik A. Ambartsumyan

Dr. Asmik A. Ambartsumyan

Nesmeyanov Institute of Organoelement Compounds RAS, Vavilov str., 28, Moscow, Russia

Search for more papers by this author
Dr. Konstantin A. Kochetkov

Dr. Konstantin A. Kochetkov

Nesmeyanov Institute of Organoelement Compounds RAS, Vavilov str., 28, Moscow, Russia

Search for more papers by this author
Prof. Dr. Tatiana V. Magdesieva

Corresponding Author

Prof. Dr. Tatiana V. Magdesieva

Chemistry Department, Lomonosov Moscow State University, Leninskie Gory 1/3, Moscow, Russia

Search for more papers by this author
First published: 01 February 2017
Citations: 3

Abstract

Stereoselective electrosynthesis of the first individual (f,tA)- and (f,tC)-1,4-fullerene derivatives with a non-inherently chiral functionalization pattern is described, as well as the first example of an optically pure protected primary amino acid directly linked to the fullerene through only the chiral α-amino-acid carbon atom. An application of an auxiliary chiral nickel-Schiff base moiety as derivatizing agent allowed separation of (f,tA)- and (f,tC)-1,4-fullerene derivatives using an achiral stationary phase, a separation which has never been done before.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.