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

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.

Affiliations

1	G.K. Boreskov Institute of Catalysis
2	Novosibirsk Institute of Organic Chemistry

Funding (1)

Russian Foundation for Basic Research

95-03-08517

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.

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

Submitted:	Mar 25, 1996
Published print:	Jul 1, 1996
Published online:	Mar 11, 2008

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