Hexa-O-acetyl-D-gentiobial in Enantioselective Synthesis of Lysocerebrosides and Their Conjugates Full article
Journal |
Mendeleev Communications
ISSN: 0959-9436 , E-ISSN: 1364-551X |
||||
---|---|---|---|---|---|
Output data | Year: 1996, Volume: 6, Number: 4, Pages: 128-130 Pages count : 3 DOI: 10.1070/MC1996v006n04ABEH000612 | ||||
Authors |
|
||||
Affiliations |
|
Funding (1)
1 | Russian Foundation for Basic Research | 95-03-08517 |
Abstract:
Hexa-O-acetyl-D-gentiobial 1 and its decyclization product (2E,4S,5R)-4-acetoxy-5-hydroxy-6-(2,3,4,6-tetra-O-acetyl-β-D-gluco-pyranosyloxy)hex-2-enal 2 have been used to synthesize O-glycosylated aminodiols 9, 10, 15 that model the structure of natural lysocerebrosides. Compounds 9, 10, 15 can serve as basic components to produce N-acylated conjugates with derivatives of arachidonic and glycyrrhizic acids.
Cite:
Tolstikov A.G.
, Tolstikova O.V.
, Tolstikov G.A.
Hexa-O-acetyl-D-gentiobial in Enantioselective Synthesis of Lysocerebrosides and Their Conjugates
Mendeleev Communications. 1996. V.6. N4. P.128-130. DOI: 10.1070/MC1996v006n04ABEH000612 WOS Scopus РИНЦ
Hexa-O-acetyl-D-gentiobial in Enantioselective Synthesis of Lysocerebrosides and Their Conjugates
Mendeleev Communications. 1996. V.6. N4. P.128-130. DOI: 10.1070/MC1996v006n04ABEH000612 WOS Scopus РИНЦ
Dates:
Submitted: | Mar 25, 1996 |
Published print: | Jul 1, 1996 |
Published online: | Mar 11, 2008 |
Identifiers:
Web of science | WOS:A1996UZ50000002 |
Scopus | 2-s2.0-27844440402 |
Elibrary | 13225433 |
Chemical Abstracts | 1996:477454 |
Chemical Abstracts (print) | 125:248276 |
OpenAlex | W1973312528 |