Synthesis of N-[(3-amino-1,2-dicarba-closo-dodecaboran-1-Yl)-acetyl] derivatives of alpha-amino acids

Authors
Levit, Galina L.Krasnov, Victor P.Gruzdev, Dmitriy A.Demin, Alexander M.Bazhov, Iliya V.Sadretdinova, Liliya Sh.Olshevskaya, Valentina A.Kalinin, Valery N.Cheong, Chan SeongChupakhin, Oleg N.Charushin, Valery N.
Issue Date
2007-12
Publisher
INST ORGANIC CHEM AND BIOCHEM
Citation
COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, v.72, no.12, pp.1697 - 1706
Abstract
The N-[(3-amino-1,2-dicarba-closo-dodecaboran-1-yl) acetyl] derivatives of alpha-amino acids were prepared starting from N-protected (Ac, Form, Bz, and Boc) 3-amino-1-(carboxymethyl)-o- carboranes and alkyl esters of natural alpha-amino acids using the carbodiimide method of coupling and removing the ester groups. All the amides obtained were diastereoisomeric mixtures. Some diastereoisomers were separated and the assignment of the absolute configuration of aminocarborane fragments was performed by X-ray crystallography.
Keywords
CHEMISTRY; CHEMISTRY; amides; N,N ' -dicyclohexylcarbodiimide; amino acids; carboranes; diastereo-isomeric resolution; HPLC; NMR spectroscopy; X-ray crystallography
ISSN
0010-0765
URI
https://pubs.kist.re.kr/handle/201004/133960
DOI
10.1135/cccc20071697
Appears in Collections:
KIST Article > 2007
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