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Stereocontrolled Synthesis of Modified Gaiactocerebroside

Alexander Genrikhovich Tolstikov 1
Alexander Genrikhovich Tolstikov
, 
Radik Khalyafovich Yamilov 2
Radik Khalyafovich Yamilov
, 
Oleg Fedorovich Prokopenko 2
Oleg Fedorovich Prokopenko
, 
Genrikh Alexandrovich Tolstikov 3
Genrikh Alexandrovich Tolstikov
10.1070/MC1992v002n03ABEH000151
Published 1992-09-30
Communication , Volume 2, Issue 3, 96-97
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Tolstikov A. G. et al. Stereocontrolled Synthesis of Modified Gaiactocerebroside // Mendeleev Communications. 1992. Vol. 2. No. 3. pp. 96-97.
GOST all authors (up to 50) Copy
Tolstikov A. G., Yamilov R. K., Prokopenko O. F., Tolstikov G. A. Stereocontrolled Synthesis of Modified Gaiactocerebroside // Mendeleev Communications. 1992. Vol. 2. No. 3. pp. 96-97.
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TY - JOUR
DO - 10.1070/MC1992v002n03ABEH000151
UR - https://mendcomm.colab.ws/publications/10.1070/MC1992v002n03ABEH000151
TI - Stereocontrolled Synthesis of Modified Gaiactocerebroside
T2 - Mendeleev Communications
AU - Tolstikov, Alexander Genrikhovich
AU - Yamilov, Radik Khalyafovich
AU - Prokopenko, Oleg Fedorovich
AU - Tolstikov, Genrikh Alexandrovich
PY - 1992
DA - 1992/09/30
PB - Mendeleev Communications
SP - 96-97
IS - 3
VL - 2
ER -
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@article{1992_Tolstikov,
author = {Alexander Genrikhovich Tolstikov and Radik Khalyafovich Yamilov and Oleg Fedorovich Prokopenko and Genrikh Alexandrovich Tolstikov},
title = {Stereocontrolled Synthesis of Modified Gaiactocerebroside},
journal = {Mendeleev Communications},
year = {1992},
volume = {2},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1992v002n03ABEH000151},
number = {3},
pages = {96--97},
doi = {10.1070/MC1992v002n03ABEH000151}
}
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Tolstikov, Alexander Genrikhovich, et al. “Stereocontrolled Synthesis of Modified Gaiactocerebroside.” Mendeleev Communications, vol. 2, no. 3, Sep. 1992, pp. 96-97. https://mendcomm.colab.ws/publications/10.1070/MC1992v002n03ABEH000151.

Abstract

Based on (4S,5R,2E)-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-6-O-acetyl-5-hydroxyhex-2-enal, (2S,3S,4E,6E)-3-O-β-d-galactopyranosyl-2-N-hexadecanoyl-8-oxo-4,6-sphingadienine has been synthesized in its pentaacetate form.