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Synthesis of glycuronamides of amino acids, constituents of microbial polysaccharides and their conversion into neoglycoconjugates of copolymer type Full article

Journal Glycoconjugate Journal
ISSN: 0282-0080 , E-ISSN: 1573-4986
Output data Year: 1991, Volume: 8, Number: 2, Pages: 82-89 Pages count : 8 DOI: 10.1007/bf00731016
Authors Chernyak Anatoly Y. 1 , Sharma Gangavaram V.M. 1 , Kononov Leonid O. 1 , Krishna Palakodety Radha 1 , Rao Alla V.Rama 2 , Kochetkov Nikolay K. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Academy of Sciences, Moscow, USSR
2 Indian Institute of Chemical Technology, Hyderabad, India.

Abstract: Glycopyranosiduronic acids, amidically linked to amino acids (alanine, serine, threonine, and lysine) were prepared.O-tert-Butyl andNε-tert-butyloxycarbonyl protected amino acidtert-butyl esters were used in ethyl 2-ethoxy-1,2-dihydroquinoline-1-carboxylate promoted condensation with 2-azidoethyl glycosides of glucuronic and galacturonic acid. Reduction of the azido-function followed byN-acryloylation and removal of blocking groups with trifluoroacetic acid gave the target monomers. These were converted into neoglycoconjugates of copolymer type, potentially useful for immunochemical studies.
Cite: Chernyak A.Y. , Sharma G.V.M. , Kononov L.O. , Krishna P.R. , Rao A.V.R. , Kochetkov N.K.
Synthesis of glycuronamides of amino acids, constituents of microbial polysaccharides and their conversion into neoglycoconjugates of copolymer type
Glycoconjugate Journal. 1991. V.8. N2. P.82-89. DOI: 10.1007/bf00731016 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:A1991FV51100004
Scopus: 2-s2.0-0026320701
OpenAlex: W2087381833
Citing:
DB Citing
OpenAlex 16
Scopus 18
Web of science 20
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