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Hexa-O-acetyl-D-gentiobial in enantioselective synthesis of lysocerebrosides and their conjugates

Alexander Genrikhovich Tolstikov 1
Alexander Genrikhovich Tolstikov
Olga V Tolstikova 2
Olga V Tolstikova
Genrikh Alexandrovich Tolstikov 2
Genrikh Alexandrovich Tolstikov
Published 1996-08-31
CommunicationVolume 6, Issue 4, 128-130
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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. Vol. 6. No. 4. pp. 128-130.
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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. Vol. 6. No. 4. pp. 128-130.
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TY - JOUR
DO - 10.1070/MC1996v006n04ABEH000612
UR - https://mendcomm.colab.ws/publications/10.1070/MC1996v006n04ABEH000612
TI - Hexa-O-acetyl-D-gentiobial in enantioselective synthesis of lysocerebrosides and their conjugates
T2 - Mendeleev Communications
AU - Tolstikov, Alexander Genrikhovich
AU - Tolstikova, Olga V
AU - Tolstikov, Genrikh Alexandrovich
PY - 1996
DA - 1996/08/31
PB - Mendeleev Communications
SP - 128-130
IS - 4
VL - 6
ER -
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@article{1996_Tolstikov,
author = {Alexander Genrikhovich Tolstikov and Olga V Tolstikova and Genrikh Alexandrovich Tolstikov},
title = {Hexa-O-acetyl-D-gentiobial in enantioselective synthesis of lysocerebrosides and their conjugates},
journal = {Mendeleev Communications},
year = {1996},
volume = {6},
publisher = {Mendeleev Communications},
month = {Aug},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1996v006n04ABEH000612},
number = {4},
pages = {128--130},
doi = {10.1070/MC1996v006n04ABEH000612}
}
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Tolstikov, Alexander Genrikhovich, et al. “Hexa-O-acetyl-D-gentiobial in enantioselective synthesis of lysocerebrosides and their conjugates.” Mendeleev Communications, vol. 6, no. 4, Aug. 1996, pp. 128-130. https://mendcomm.colab.ws/publications/10.1070/MC1996v006n04ABEH000612.

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.

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