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Hexa-O-acetyl-D-gentiobial in Enantioselective Synthesis of Lysocerebrosides and Their Conjugates Full article

Общее Language: Английский, Genre: Full article,
Status: Published, Source type: Original
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 Tolstikov Aleksander G. 1 , Tolstikova Olga V. 1 , Tolstikov Genrikh A. 2
Affiliations
1 G.K. Boreskov Institute of Catalysis
2 Novosibirsk Institute of Organic Chemistry

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 publication_identifier_short.wos_identifier_type publication_identifier_short.scopus_identifier_type publication_identifier_short.rinz_identifier_type
Dates:
Submitted: Mar 25, 1996
Published print: Jul 1, 1996
Published online: Mar 11, 2008
Identifiers:
publication_identifier.wos_identifier_type WOS:A1996UZ50000002
publication_identifier.scopus_identifier_type 2-s2.0-27844440402
publication_identifier.rinz_identifier_type 13225433
publication_identifier.accession_number_identifier_type 1996:477454
publication_identifier.chemical_accession_number_identifier_type 125:248276
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