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Synthesis of spacered derivatives of β-lactosylamine with an amino function at the terminal position of an aglycon Full article

Journal Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Output data Year: 2006, Volume: 55, Number: 7, Pages: 1262-1267 Pages count : 6 DOI: 10.1007/s11172-006-0409-6
Authors Likhosherstov L.M. 1 , Novikova O.S. 1 , Kononov L.O. 1 , Shibaev V.N. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

Abstract: A set of N-acyllactosylamine derivatives containing a terminal amino group in aglycons of various lengths (up to 16 atoms) and various hydrophilicities were synthesized. The aglycons were represented by di-, tri-, and pentapeptides containing glycine and serine residues and by aglycons containing fragments of tartaric acid or a tertiary amine.
Cite: Likhosherstov L.M. , Novikova O.S. , Kononov L.O. , Shibaev V.N.
Synthesis of spacered derivatives of β-lactosylamine with an amino function at the terminal position of an aglycon
Russian Chemical Bulletin. 2006. V.55. N7. P.1262-1267. DOI: 10.1007/s11172-006-0409-6 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000242918900025
Scopus: 2-s2.0-33751572167
OpenAlex: W2949190044
Citing:
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OpenAlex 3
Scopus 3
Web of science 5
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