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 |
|
||||
| Affiliations |
|
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
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 |